Canonical Allele Identifier: CA2270161110
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941805T= , CM000679.2:g.63941805T= GRCh38
NC_000017.10:g.62019165T= , CM000679.1:g.62019165T= GRCh37
NC_000017.9:g.59372897T= NCBI36
NG_011699.1:g.36114A=

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.4477A= MANE Select ENSP00000396320.1:p.Met1493=
ENST00000578147.5:c.4477A= ENSP00000463963.1:p.Met1493=
NM_000334.4:c.4477A= MANE Select NP_000325.4:p.Met1493=
XM_005257566.3:c.4477A= XP_005257623.1:p.Met1493=