Canonical Allele Identifier: CA8709256
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs762093872

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63945648A>T , CM000679.2:g.63945648A>T GRCh38
NC_000017.10:g.62023008A>T , CM000679.1:g.62023008A>T GRCh37
NC_000017.9:g.59376740A>T NCBI36
NG_011699.1:g.32271T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3442-10T>A MANE Select ENSP00000396320.1:n.3442-10T>A
ENST00000578147.5:c.3442-10T>A ENSP00000463963.1:n.3442-10T>A
NM_000334.4:c.3442-10T>A MANE Select NP_000325.4:n.3442-10T>A
XM_005257566.3:c.3442-10T>A XP_005257623.1:n.3442-10T>A