Canonical Allele Identifier: CA8709689
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs80338788

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63959269C>A , CM000679.2:g.63959269C>A GRCh38
NC_000017.10:g.62036629C>A , CM000679.1:g.62036629C>A GRCh37
NC_000017.9:g.59390361C>A NCBI36
NG_011699.1:g.18650G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.2015G>T MANE Select ENSP00000396320.1:p.Arg672Leu
ENST00000578147.5:c.2015G>T ENSP00000463963.1:p.Arg672Leu
NM_000334.4:c.2015G>T MANE Select NP_000325.4:p.Arg672Leu
XM_005257566.3:c.2015G>T XP_005257623.1:p.Arg672Leu