Canonical Allele Identifier: CA2270173940
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63968232A= , CM000679.2:g.63968232A= GRCh38
NC_000017.10:g.62045592A= , CM000679.1:g.62045592A= GRCh37
NC_000017.9:g.59399324A= NCBI36
NG_011699.1:g.9687T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.827T= MANE Select ENSP00000396320.1:p.Leu276=
ENST00000578147.5:c.827T= ENSP00000463963.1:p.Leu276=
NM_000334.4:c.827T= MANE Select NP_000325.4:p.Leu276=
XM_005257566.3:c.827T= XP_005257623.1:p.Leu276=