Canonical Allele Identifier: CA117854
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 5922
dbSNP Id: rs121908560

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63944694G>T , CM000679.2:g.63944694G>T GRCh38
NC_000017.10:g.62022054G>T , CM000679.1:g.62022054G>T GRCh37
NC_000017.9:g.59375786G>T NCBI36
NG_011699.1:g.33225C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3891C>A MANE Select ENSP00000396320.1:p.Asn1297Lys
ENST00000578147.5:c.3891C>A ENSP00000463963.1:p.Asn1297Lys
NM_000334.4:c.3891C>A MANE Select NP_000325.4:p.Asn1297Lys
XM_005257566.3:c.3891C>A XP_005257623.1:p.Asn1297Lys