Canonical Allele Identifier: CA400613434
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941073C>G , CM000679.2:g.63941073C>G GRCh38
NC_000017.10:g.62018433C>G , CM000679.1:g.62018433C>G GRCh37
NC_000017.9:g.59372165C>G NCBI36
NG_011699.1:g.36846G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.5209G>C MANE Select ENSP00000396320.1:p.Ala1737Pro
ENST00000578147.5:c.5209G>C ENSP00000463963.1:p.Ala1737Pro
NM_000334.4:c.5209G>C MANE Select NP_000325.4:p.Ala1737Pro
XM_005257566.3:c.5209G>C XP_005257623.1:p.Ala1737Pro