Canonical Allele Identifier: CA2148899280
Gene: NRXN3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.78544906_78544907delinsAG , CM000676.2:g.78544906_78544907delinsAG GRCh38
NC_000014.8:g.79011249_79011250delinsAG , CM000676.1:g.79011249_79011250delinsAG GRCh37
NC_000014.7:g.78081002_78081003delinsAG NCBI36
NG_052991.1:g.379534_379535delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000335750.7:c.758-100214_758-100213delinsAG MANE Select ENSP00000338349.7:n.758-100214_758-100213delinsAG
ENST00000553363.6:c.49-100214_49-100213delinsAG
ENST00000634499.2:c.770-100214_770-100213delinsAG ENSP00000488920.2:n.770-100214_770-100213delinsAG
ENST00000553363.5:c.51-100214_51-100213delinsAG
ENST00000553631.1:c.-136-57514_-136-57513delinsAG ENSP00000451947.1:n.-136-57514_-136-57513delinsAG
ENST00000554719.5:c.-362-100214_-362-100213delinsAG ENSP00000451648.1:n.-362-100214_-362-100213delinsAG
ENST00000554738.5:c.752-100214_752-100213delinsAG ENSP00000450683.1:n.752-100214_752-100213delinsAG
ENST00000556088.1:n.250-100214_250-100213delinsAG
ENST00000634499.1:c.752-100214_752-100213delinsAG ENSP00000488920.1:n.752-100214_752-100213delinsAG
ENST00000635466.1:c.758-100214_758-100213delinsAG ENSP00000489551.1:n.758-100214_758-100213delinsAG
NM_004796.5:c.-362-100214_-362-100213delinsAG NP_004787.2:n.-362-100214_-362-100213delinsAG
NR_073547.1:n.1757-100214_1757-100213delinsAG
XM_005268218.2:c.770-100214_770-100213delinsAG XP_005268275.1:n.770-100214_770-100213delinsAG
XM_006720322.2:c.758-100214_758-100213delinsAG XP_006720385.1:n.758-100214_758-100213delinsAG
XM_006720323.2:c.758-100214_758-100213delinsAG XP_006720386.1:n.758-100214_758-100213delinsAG
XM_011537363.1:c.770-100214_770-100213delinsAG XP_011535665.1:n.770-100214_770-100213delinsAG
XM_011537364.1:c.770-100214_770-100213delinsAG XP_011535666.1:n.770-100214_770-100213delinsAG
XM_011537365.1:c.770-100214_770-100213delinsAG XP_011535667.1:n.770-100214_770-100213delinsAG
XM_011537366.1:c.770-100214_770-100213delinsAG XP_011535668.1:n.770-100214_770-100213delinsAG
XM_011537367.1:c.770-100214_770-100213delinsAG XP_011535669.1:n.770-100214_770-100213delinsAG
XM_011537368.1:c.770-100214_770-100213delinsAG XP_011535670.1:n.770-100214_770-100213delinsAG
XM_011537369.1:c.770-100214_770-100213delinsAG XP_011535671.1:n.770-100214_770-100213delinsAG
XM_011537370.1:c.770-100214_770-100213delinsAG XP_011535672.1:n.770-100214_770-100213delinsAG
XM_011537371.1:c.770-100214_770-100213delinsAG XP_011535673.1:n.770-100214_770-100213delinsAG
XM_011537372.1:c.770-100214_770-100213delinsAG XP_011535674.1:n.770-100214_770-100213delinsAG
XM_011537373.1:c.770-100214_770-100213delinsAG XP_011535675.1:n.770-100214_770-100213delinsAG
XM_011537374.1:c.770-100214_770-100213delinsAG XP_011535676.1:n.770-100214_770-100213delinsAG
XM_011537375.1:c.770-100214_770-100213delinsAG XP_011535677.1:n.770-100214_770-100213delinsAG
XM_011537376.1:c.770-100214_770-100213delinsAG XP_011535678.1:n.770-100214_770-100213delinsAG
XM_011537377.1:c.-323-100214_-323-100213delinsAG XP_011535679.1:n.-323-100214_-323-100213delinsAG
XR_943561.1:n.1775-100214_1775-100213delinsAG
XR_943562.1:n.1775-100214_1775-100213delinsAG
XR_943563.1:n.1775-100214_1775-100213delinsAG
NM_001330195.1:c.758-100214_758-100213delinsAG NP_001317124.1:n.758-100214_758-100213delinsAG
NM_001366425.1:c.758-100214_758-100213delinsAG NP_001353354.1:n.758-100214_758-100213delinsAG
NM_001366426.1:c.770-100214_770-100213delinsAG NP_001353355.1:n.770-100214_770-100213delinsAG
NR_158973.1:n.1775-100214_1775-100213delinsAG
NR_158974.1:n.1763-100214_1763-100213delinsAG
NR_158975.1:n.1775-100214_1775-100213delinsAG
XM_005268218.3:c.770-100214_770-100213delinsAG XP_005268275.1:n.770-100214_770-100213delinsAG
XM_011537364.2:c.770-100214_770-100213delinsAG XP_011535666.1:n.770-100214_770-100213delinsAG
XM_011537365.2:c.770-100214_770-100213delinsAG XP_011535667.1:n.770-100214_770-100213delinsAG
XM_017021790.1:c.770-100214_770-100213delinsAG XP_016877279.1:n.770-100214_770-100213delinsAG
XM_017021791.1:c.770-100214_770-100213delinsAG XP_016877280.1:n.770-100214_770-100213delinsAG
XM_017021792.1:c.758-100214_758-100213delinsAG XP_016877281.1:n.758-100214_758-100213delinsAG
XM_017021793.1:c.770-100214_770-100213delinsAG XP_016877282.1:n.770-100214_770-100213delinsAG
XM_017021794.1:c.758-100214_758-100213delinsAG XP_016877283.1:n.758-100214_758-100213delinsAG
XM_017021796.2:c.770-100214_770-100213delinsAG XP_016877285.1:n.770-100214_770-100213delinsAG
XM_017021797.1:c.710-100214_710-100213delinsAG XP_016877286.1:n.710-100214_710-100213delinsAG
XM_017021798.1:c.758-100214_758-100213delinsAG XP_016877287.1:n.758-100214_758-100213delinsAG
XM_017021799.2:c.770-100214_770-100213delinsAG XP_016877288.1:n.770-100214_770-100213delinsAG
XM_017021800.1:c.770-100214_770-100213delinsAG XP_016877289.1:n.770-100214_770-100213delinsAG
XM_017021801.1:c.770-100214_770-100213delinsAG XP_016877290.1:n.770-100214_770-100213delinsAG
XM_017021804.1:c.770-100214_770-100213delinsAG XP_016877293.1:n.770-100214_770-100213delinsAG
XM_017021805.1:c.758-100214_758-100213delinsAG XP_016877294.1:n.758-100214_758-100213delinsAG
XM_017021807.1:c.770-100214_770-100213delinsAG XP_016877296.1:n.770-100214_770-100213delinsAG
XM_024449750.1:c.770-100214_770-100213delinsAG XP_024305518.1:n.770-100214_770-100213delinsAG
XM_024449751.1:c.758-100214_758-100213delinsAG XP_024305519.1:n.758-100214_758-100213delinsAG
XM_024449752.1:c.758-100214_758-100213delinsAG XP_024305520.1:n.758-100214_758-100213delinsAG
XM_024449753.1:c.758-100214_758-100213delinsAG XP_024305521.1:n.758-100214_758-100213delinsAG
XR_001750599.1:n.1775-100214_1775-100213delinsAG
XR_001750600.1:n.1775-100214_1775-100213delinsAG
XR_001750602.1:n.1775-100214_1775-100213delinsAG
XR_001750604.1:n.1775-100214_1775-100213delinsAG
XR_001750605.1:n.1775-100214_1775-100213delinsAG
XR_001750606.1:n.1775-100214_1775-100213delinsAG
XR_001750607.1:n.1775-100214_1775-100213delinsAG
XR_001750609.1:n.1775-100214_1775-100213delinsAG
XR_001750610.1:n.1775-100214_1775-100213delinsAG
XR_002957572.1:n.1775-100214_1775-100213delinsAG
XR_943563.2:n.1775-100214_1775-100213delinsAG
NM_001330195.2:c.758-100214_758-100213delinsAG MANE Select NP_001317124.1:n.758-100214_758-100213delinsAG
NM_004796.6:c.-362-100214_-362-100213delinsAG NP_004787.2:n.-362-100214_-362-100213delinsAG
NR_073547.2:n.1757-100214_1757-100213delinsAG
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