Canonical Allele Identifier: CA2639322252
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941058_63941096dup , CM000679.2:g.63941058_63941096dup GRCh38
NC_000017.10:g.62018418_62018456dup , CM000679.1:g.62018418_62018456dup GRCh37
NC_000017.9:g.59372150_59372188dup NCBI36
NG_011699.1:g.36825_36863dup

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.5188_5226dup MANE Select ENSP00000396320.1:p.Leu1742_Leu1743insCys...
ENST00000578147.5:c.5188_5226dup ENSP00000463963.1:p.Leu1742_Leu1743insCys...
NM_000334.4:c.5188_5226dup MANE Select NP_000325.4:p.Leu1742_Leu1743insCysAlaIle...
XM_005257566.3:c.5188_5226dup XP_005257623.1:p.Leu1742_Leu1743insCysAla...