Canonical Allele Identifier: CA645373129
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 21158
ClinVar RCV Id: RCV000020275

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.[63941803C>T;63941814A>G] , CM000679.2:g.[63941803C>T;63941814A>G] GRCh38
NC_000017.10:g.[62019163C>T;62019174A>G] , CM000679.1:g.[62019163C>T;62019174A>G] GRCh37
NC_000017.9:g.[59372895C>T;59372906A>G] NCBI36
NG_011699.1:g.[36105T>C;36116G>A]

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.[4468T>C;4479G>A] MANE Select ENSP00000396320.1:p.[Phe1490Leu;Met1493Il...
ENST00000578147.5:c.[4468T>C;4479G>A] ENSP00000463963.1:p.[Phe1490Leu;Met1493Il...
NM_000334.4:c.[4468T>C;4479G>A] MANE Select NP_000325.4:p.[Phe1490Leu;Met1493Ile]
XM_005257566.3:c.[4468T>C;4479G>A] XP_005257623.1:p.[Phe1490Leu;Met1493Ile]