Canonical Allele Identifier: CA501217687
Gene: SCN4A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.62022036C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63944676C>T , CM000679.2:g.63944676C>T GRCh38
NC_000017.10:g.62022036C>T , CM000679.1:g.62022036C>T GRCh37
NC_000017.9:g.59375768C>T NCBI36
NG_011699.1:g.33243G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3909G>A MANE Select ENSP00000396320.1:p.Lys1303=
ENST00000578147.5:c.3909G>A ENSP00000463963.1:p.Lys1303=
NM_000334.4:c.3909G>A MANE Select NP_000325.4:p.Lys1303=
XM_005257566.3:c.3909G>A XP_005257623.1:p.Lys1303=
Search 100 bp 5'
Search 100 bp 3'