Canonical Allele Identifier: CA2270162389

Gene: SCN4A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63944319A= , CM000679.2:g.63944319A=	GRCh38
NC_000017.10:g.62021679A= , CM000679.1:g.62021679A=	GRCh37
NC_000017.9:g.59375411A=	NCBI36
NG_011699.1:g.33600T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435607.3:c.3912+354T= MANE Select	ENSP00000396320.1:n.3912+354T=
ENST00000578147.5:c.3916+350T=	ENSP00000463963.1:n.3916+350T=
NM_000334.4:c.3912+354T= MANE Select	NP_000325.4:n.3912+354T=
XM_005257566.3:c.3912+354T=	XP_005257623.1:n.3912+354T=