Canonical Allele Identifier: CA2639314735

Gene: SCN4A

Linked Data

• gnomAD v4: 17-63947008-A-AAACCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63947008_63947009insAACCC , CM000679.2:g.63947008_63947009insAACCC	GRCh38
NC_000017.10:g.62024368_62024369insAACCC , CM000679.1:g.62024368_62024369insAACCC	GRCh37
NC_000017.9:g.59378100_59378101insAACCC	NCBI36
NG_011699.1:g.30910_30911insGGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435607.3:c.3441+36_3441+37insGGGTT MANE Select	ENSP00000396320.1:n.3441+36_3441+37insGGGTT
ENST00000578147.5:c.3441+36_3441+37insGGGTT	ENSP00000463963.1:n.3441+36_3441+37insGGGTT
NM_000334.4:c.3441+36_3441+37insGGGTT MANE Select	NP_000325.4:n.3441+36_3441+37insGGGTT
XM_005257566.3:c.3441+36_3441+37insGGGTT	XP_005257623.1:n.3441+36_3441+37insGGGTT