Canonical Allele Identifier: CA15828862
Gene: NRXN3 HGNC NCBI

Linked Data

dbSNP Id: rs10146997

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.79478819A>G , CM000676.2:g.79478819A>G GRCh38
NC_000014.8:g.79945162A>G , CM000676.1:g.79945162A>G GRCh37
NC_000014.7:g.79014915A>G NCBI36
NG_052991.1:g.1313447A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000281127.11:c.429+11417A>G ENSP00000281127.7:p.=
ENST00000428277.6:c.429+11417A>G ENSP00000394426.2:p.=
ENST00000554719.5:c.2325+11417A>G ENSP00000451648.1:p.=
ENST00000554738.5:c.3411+11417A>G ENSP00000450683.1:p.=
ENST00000555387.1:c.429+11417A>G ENSP00000451393.1:p.=
ENST00000557594.5:c.429+11417A>G ENSP00000451672.1:p.=
ENST00000634499.1:c.3411+11417A>G ENSP00000488920.1:p.=
ENST00000635466.1:c.3444+11417A>G ENSP00000489551.1:p.=
NM_001105250.2:c.429+11417A>G NP_001098720.1:p.=
NM_001272020.1:c.429+11417A>G NP_001258949.1:p.=
NM_004796.5:c.2325+11417A>G NP_004787.2:p.=
NM_138970.4:c.429+11417A>G NP_620426.2:p.=
XM_005268218.2:c.3480+11417A>G XP_005268275.1:p.=
XM_006720322.2:c.3468+11417A>G XP_006720385.1:p.=
XM_006720323.2:c.3444+11417A>G XP_006720386.1:p.=
XM_011537363.1:c.3480+11417A>G XP_011535665.1:p.=
XM_011537364.1:c.3480+11417A>G XP_011535666.1:p.=
XM_011537365.1:c.3480+11417A>G XP_011535667.1:p.=
XM_011537366.1:c.3456+11417A>G XP_011535668.1:p.=
XM_011537367.1:c.3480+11417A>G XP_011535669.1:p.=
XM_011537368.1:c.3480+11417A>G XP_011535670.1:p.=
XM_011537369.1:c.3480+11417A>G XP_011535671.1:p.=
XM_011537370.1:c.3456+11417A>G XP_011535672.1:p.=
XM_011537371.1:c.3480+11417A>G XP_011535673.1:p.=
XM_011537372.1:c.3480+11417A>G XP_011535674.1:p.=
XM_011537373.1:c.3480+11417A>G XP_011535675.1:p.=
XM_011537374.1:c.3480+11417A>G XP_011535676.1:p.=
XM_011537375.1:c.3480+11417A>G XP_011535677.1:p.=
XM_011537376.1:c.3480+11417A>G XP_011535678.1:p.=
XM_011537377.1:c.2388+11417A>G XP_011535679.1:p.=
NM_001330195.1:c.3444+11417A>G NP_001317124.1:p.=
NM_001366425.1:c.3444+11417A>G NP_001353354.1:p.=
NM_001366426.1:c.3456+11417A>G NP_001353355.1:p.=
XM_005268218.3:c.3480+11417A>G XP_005268275.1:p.=
XM_011537364.2:c.3480+11417A>G XP_011535666.1:p.=
XM_011537365.2:c.3480+11417A>G XP_011535667.1:p.=
XM_017021790.1:c.3480+11417A>G XP_016877279.1:p.=
XM_017021791.1:c.3480+11417A>G XP_016877280.1:p.=
XM_017021792.1:c.3468+11417A>G XP_016877281.1:p.=
XM_017021793.1:c.3453+11417A>G XP_016877282.1:p.=
XM_017021794.1:c.3444+11417A>G XP_016877283.1:p.=
XM_017021796.2:c.3429+11417A>G XP_016877285.1:p.=
XM_017021797.1:c.3420+11417A>G XP_016877286.1:p.=
XM_017021798.1:c.3417+11417A>G XP_016877287.1:p.=
XM_017021799.2:c.3480+11417A>G XP_016877288.1:p.=
XM_017021800.1:c.3480+11417A>G XP_016877289.1:p.=
XM_017021801.1:c.3453+11417A>G XP_016877290.1:p.=
XM_017021804.1:c.3453+11417A>G XP_016877293.1:p.=
XM_017021805.1:c.3444+11417A>G XP_016877294.1:p.=
XM_017021807.1:c.3480+11417A>G XP_016877296.1:p.=
XM_024449750.1:c.3453+11417A>G XP_024305518.1:p.=
XM_024449751.1:c.3417+11417A>G XP_024305519.1:p.=
XM_024449752.1:c.3468+11417A>G XP_024305520.1:p.=
XM_024449753.1:c.3417+11417A>G XP_024305521.1:p.=
NM_001105250.3:c.429+11417A>G NP_001098720.1:p.=
NM_001272020.2:c.429+11417A>G NP_001258949.1:p.=
NM_001330195.2:c.3444+11417A>G MANE Select NP_001317124.1:p.=
NM_004796.6:c.2325+11417A>G NP_004787.2:p.=
NM_138970.5:c.429+11417A>G NP_620426.2:p.=