Canonical Allele Identifier: CA292962584
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs34902492

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63947259dup , CM000679.2:g.63947259dup GRCh38
NC_000017.10:g.62024619dup , CM000679.1:g.62024619dup GRCh37
NC_000017.9:g.59378351dup NCBI36
NG_011699.1:g.30661dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3319-91dup MANE Select ENSP00000396320.1:n.3319-91dup
ENST00000578147.5:c.3319-91dup ENSP00000463963.1:n.3319-91dup
NM_000334.4:c.3319-91dup MANE Select NP_000325.4:n.3319-91dup
XM_005257566.3:c.3319-91dup XP_005257623.1:n.3319-91dup