Canonical Allele Identifier: CA400614552
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941369C>A , CM000679.2:g.63941369C>A GRCh38
NC_000017.10:g.62018729C>A , CM000679.1:g.62018729C>A GRCh37
NC_000017.9:g.59372461C>A NCBI36
NG_011699.1:g.36550G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.4913G>T MANE Select ENSP00000396320.1:p.Ser1638Ile
ENST00000578147.5:c.4913G>T ENSP00000463963.1:p.Ser1638Ile
NM_000334.4:c.4913G>T MANE Select NP_000325.4:p.Ser1638Ile
XM_005257566.3:c.4913G>T XP_005257623.1:p.Ser1638Ile