Canonical Allele Identifier: CA2270161420

Gene: SCN4A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63942321G= , CM000679.2:g.63942321G=	GRCh38
NC_000017.10:g.62019681G= , CM000679.1:g.62019681G=	GRCh37
NC_000017.9:g.59373413G=	NCBI36
NG_011699.1:g.35598C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435607.3:c.4289-328C= MANE Select	ENSP00000396320.1:n.4289-328C=
ENST00000578147.5:c.4289-328C=	ENSP00000463963.1:n.4289-328C=
NM_000334.4:c.4289-328C= MANE Select	NP_000325.4:n.4289-328C=
XM_005257566.3:c.4289-328C=	XP_005257623.1:n.4289-328C=