Canonical Allele Identifier: CA264212821

Gene: NRXN3

Linked Data

• dbSNP Id: rs779219681
• gnomAD v3: 14-79518162-C-T
• gnomAD v4: 14-79518162-C-T
• MyVariant Identifiers: chr14:g.79984505C>T (hg19) ; chr14:g.79518162C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.79518162C>T , CM000676.2:g.79518162C>T	GRCh38
NC_000014.8:g.79984505C>T , CM000676.1:g.79984505C>T	GRCh37
NC_000014.7:g.79054258C>T	NCBI36
NG_052991.1:g.1352790C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335750.7:c.3444+50760C>T MANE Select	ENSP00000338349.7:n.3444+50760C>T
ENST00000634499.2:c.3456+50760C>T	ENSP00000488920.2:n.3456+50760C>T
ENST00000635466.2:c.2714+50760C>T
ENST00000676811.1:c.429+50760C>T	ENSP00000504450.1:n.429+50760C>T
ENST00000679122.1:c.429+50760C>T	ENSP00000502844.1:n.429+50760C>T
ENST00000281127.11:c.429+50760C>T	ENSP00000281127.7:n.429+50760C>T
ENST00000428277.6:c.429+50760C>T	ENSP00000394426.2:n.429+50760C>T
ENST00000553803.5:n.296+50760C>T
ENST00000554719.5:c.2325+50760C>T	ENSP00000451648.1:n.2325+50760C>T
ENST00000554738.5:c.3411+50760C>T	ENSP00000450683.1:n.3411+50760C>T
ENST00000555073.5:n.395+50760C>T
ENST00000555387.1:c.429+50760C>T	ENSP00000451393.1:n.429+50760C>T
ENST00000556003.1:n.281+50760C>T
ENST00000557594.5:c.429+50760C>T	ENSP00000451672.1:n.429+50760C>T
ENST00000634499.1:c.3411+50760C>T	ENSP00000488920.1:n.3411+50760C>T
ENST00000635466.1:c.3444+50760C>T	ENSP00000489551.1:n.3444+50760C>T
NM_001105250.2:c.429+50760C>T	NP_001098720.1:n.429+50760C>T
NM_001272020.1:c.429+50760C>T	NP_001258949.1:n.429+50760C>T
NM_004796.5:c.2325+50760C>T	NP_004787.2:n.2325+50760C>T
NM_138970.4:c.429+50760C>T	NP_620426.2:n.429+50760C>T
NR_073546.1:n.1382+50760C>T
NR_073547.1:n.4416+50760C>T
XM_005268218.2:c.3480+50760C>T	XP_005268275.1:n.3480+50760C>T
XM_006720322.2:c.3468+50760C>T	XP_006720385.1:n.3468+50760C>T
XM_006720323.2:c.3444+50760C>T	XP_006720386.1:n.3444+50760C>T
XM_011537363.1:c.3480+50760C>T	XP_011535665.1:n.3480+50760C>T
XM_011537364.1:c.3480+50760C>T	XP_011535666.1:n.3480+50760C>T
XM_011537365.1:c.3480+50760C>T	XP_011535667.1:n.3480+50760C>T
XM_011537366.1:c.3456+50760C>T	XP_011535668.1:n.3456+50760C>T
XM_011537367.1:c.3480+50760C>T	XP_011535669.1:n.3480+50760C>T
XM_011537368.1:c.3480+50760C>T	XP_011535670.1:n.3480+50760C>T
XM_011537369.1:c.3480+50760C>T	XP_011535671.1:n.3480+50760C>T
XM_011537370.1:c.3456+50760C>T	XP_011535672.1:n.3456+50760C>T
XM_011537371.1:c.3480+50760C>T	XP_011535673.1:n.3480+50760C>T
XM_011537372.1:c.3480+50760C>T	XP_011535674.1:n.3480+50760C>T
XM_011537373.1:c.3480+50760C>T	XP_011535675.1:n.3480+50760C>T
XM_011537374.1:c.3480+50760C>T	XP_011535676.1:n.3480+50760C>T
XM_011537375.1:c.3480+50760C>T	XP_011535677.1:n.3480+50760C>T
XM_011537376.1:c.3480+50760C>T	XP_011535678.1:n.3480+50760C>T
XM_011537377.1:c.2388+50760C>T	XP_011535679.1:n.2388+50760C>T
XR_943561.1:n.4485+50760C>T
XR_943562.1:n.4485+50760C>T
XR_943563.1:n.4485+50760C>T
NM_001330195.1:c.3444+50760C>T	NP_001317124.1:n.3444+50760C>T
NM_001366425.1:c.3444+50760C>T	NP_001353354.1:n.3444+50760C>T
NM_001366426.1:c.3456+50760C>T	NP_001353355.1:n.3456+50760C>T
NR_158973.1:n.4461+50760C>T
NR_158974.1:n.4449+50760C>T
NR_158975.1:n.4461+50760C>T
XM_005268218.3:c.3480+50760C>T	XP_005268275.1:n.3480+50760C>T
XM_011537364.2:c.3480+50760C>T	XP_011535666.1:n.3480+50760C>T
XM_011537365.2:c.3480+50760C>T	XP_011535667.1:n.3480+50760C>T
XM_017021790.1:c.3480+50760C>T	XP_016877279.1:n.3480+50760C>T
XM_017021791.1:c.3480+50760C>T	XP_016877280.1:n.3480+50760C>T
XM_017021792.1:c.3468+50760C>T	XP_016877281.1:n.3468+50760C>T
XM_017021793.1:c.3453+50760C>T	XP_016877282.1:n.3453+50760C>T
XM_017021794.1:c.3444+50760C>T	XP_016877283.1:n.3444+50760C>T
XM_017021796.2:c.3429+50760C>T	XP_016877285.1:n.3429+50760C>T
XM_017021797.1:c.3420+50760C>T	XP_016877286.1:n.3420+50760C>T
XM_017021798.1:c.3417+50760C>T	XP_016877287.1:n.3417+50760C>T
XM_017021799.2:c.3480+50760C>T	XP_016877288.1:n.3480+50760C>T
XM_017021800.1:c.3480+50760C>T	XP_016877289.1:n.3480+50760C>T
XM_017021801.1:c.3453+50760C>T	XP_016877290.1:n.3453+50760C>T
XM_017021804.1:c.3453+50760C>T	XP_016877293.1:n.3453+50760C>T
XM_017021805.1:c.3444+50760C>T	XP_016877294.1:n.3444+50760C>T
XM_017021807.1:c.3480+50760C>T	XP_016877296.1:n.3480+50760C>T
XM_024449750.1:c.3453+50760C>T	XP_024305518.1:n.3453+50760C>T
XM_024449751.1:c.3417+50760C>T	XP_024305519.1:n.3417+50760C>T
XM_024449752.1:c.3468+50760C>T	XP_024305520.1:n.3468+50760C>T
XM_024449753.1:c.3417+50760C>T	XP_024305521.1:n.3417+50760C>T
XR_001750599.1:n.4485+50760C>T
XR_001750600.1:n.4485+50760C>T
XR_001750602.1:n.4458+50760C>T
XR_001750604.1:n.4434+50760C>T
XR_001750605.1:n.4434+50760C>T
XR_001750606.1:n.4485+50760C>T
XR_001750607.1:n.4485+50760C>T
XR_001750609.1:n.4485+50760C>T
XR_001750610.1:n.4485+50760C>T
XR_002957572.1:n.4485+50760C>T
XR_943563.2:n.4485+50760C>T
NM_001105250.3:c.429+50760C>T	NP_001098720.1:n.429+50760C>T
NM_001272020.2:c.429+50760C>T	NP_001258949.1:n.429+50760C>T
NM_001330195.2:c.3444+50760C>T MANE Select	NP_001317124.1:n.3444+50760C>T
NM_004796.6:c.2325+50760C>T	NP_004787.2:n.2325+50760C>T
NM_138970.5:c.429+50760C>T	NP_620426.2:n.429+50760C>T
NR_073546.2:n.1341+50760C>T
NR_073547.2:n.4416+50760C>T