Canonical Allele Identifier: CA2270168621
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63957331T= , CM000679.2:g.63957331T= GRCh38
NC_000017.10:g.62034691T= , CM000679.1:g.62034691T= GRCh37
NC_000017.9:g.59388423T= NCBI36
NG_011699.1:g.20588A=

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.2207A= MANE Select ENSP00000396320.1:p.Asp736=
ENST00000578147.5:c.2207A= ENSP00000463963.1:p.Asp736=
NM_000334.4:c.2207A= MANE Select NP_000325.4:p.Asp736=
XM_005257566.3:c.2207A= XP_005257623.1:p.Asp736=