Canonical Allele Identifier: CA2639314666

Gene: SCN4A

Linked Data

• gnomAD v4: 17-63947007-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63947007_63947008insCT , CM000679.2:g.63947007_63947008insCT	GRCh38
NC_000017.10:g.62024367_62024368insCT , CM000679.1:g.62024367_62024368insCT	GRCh37
NC_000017.9:g.59378099_59378100insCT	NCBI36
NG_011699.1:g.30911_30912insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435607.3:c.3441+37_3441+38insAG MANE Select	ENSP00000396320.1:n.3441+37_3441+38insAG
ENST00000578147.5:c.3441+37_3441+38insAG	ENSP00000463963.1:n.3441+37_3441+38insAG
NM_000334.4:c.3441+37_3441+38insAG MANE Select	NP_000325.4:n.3441+37_3441+38insAG
XM_005257566.3:c.3441+37_3441+38insAG	XP_005257623.1:n.3441+37_3441+38insAG