Canonical Allele Identifier: CA400617479
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs1257080690

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63944792A>G , CM000679.2:g.63944792A>G GRCh38
NC_000017.10:g.62022152A>G , CM000679.1:g.62022152A>G GRCh37
NC_000017.9:g.59375884A>G NCBI36
NG_011699.1:g.33127T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3793T>C MANE Select ENSP00000396320.1:p.Tyr1265His
ENST00000578147.5:c.3793T>C ENSP00000463963.1:p.Tyr1265His
NM_000334.4:c.3793T>C MANE Select NP_000325.4:p.Tyr1265His
XM_005257566.3:c.3793T>C XP_005257623.1:p.Tyr1265His