Canonical Allele Identifier: CA2639311016
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63971922dup , CM000679.2:g.63971922dup GRCh38
NC_000017.10:g.62049282dup , CM000679.1:g.62049282dup GRCh37
NC_000017.9:g.59403014dup NCBI36
NG_011699.1:g.6001dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.483-68dup MANE Select ENSP00000396320.1:n.483-68dup
ENST00000578147.5:c.483-68dup ENSP00000463963.1:n.483-68dup
NM_000334.4:c.483-68dup MANE Select NP_000325.4:n.483-68dup
XM_005257566.3:c.483-68dup XP_005257623.1:n.483-68dup