Canonical Allele Identifier: CA400631374
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs751368967

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63957493G>T , CM000679.2:g.63957493G>T GRCh38
NC_000017.10:g.62034853G>T , CM000679.1:g.62034853G>T GRCh37
NC_000017.9:g.59388585G>T NCBI36
NG_011699.1:g.20426C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.2045C>A MANE Select ENSP00000396320.1:p.Ser682Ter
ENST00000578147.5:c.2045C>A ENSP00000463963.1:p.Ser682Ter
NM_000334.4:c.2045C>A MANE Select NP_000325.4:p.Ser682Ter
XM_005257566.3:c.2045C>A XP_005257623.1:p.Ser682Ter