Canonical Allele Identifier: CA400620580
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs548721699

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63947119C>A , CM000679.2:g.63947119C>A GRCh38
NC_000017.10:g.62024479C>A , CM000679.1:g.62024479C>A GRCh37
NC_000017.9:g.59378211C>A NCBI36
NG_011699.1:g.30800G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3367G>T MANE Select ENSP00000396320.1:p.Gly1123Ter
ENST00000578147.5:c.3367G>T ENSP00000463963.1:p.Gly1123Ter
NM_000334.4:c.3367G>T MANE Select NP_000325.4:p.Gly1123Ter
XM_005257566.3:c.3367G>T XP_005257623.1:p.Gly1123Ter