Canonical Allele Identifier: CA400633161
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63961285T>G , CM000679.2:g.63961285T>G GRCh38
NC_000017.10:g.62038645T>G , CM000679.1:g.62038645T>G GRCh37
NC_000017.9:g.59392377T>G NCBI36
NG_011699.1:g.16634A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.1753A>C MANE Select ENSP00000396320.1:p.Thr585Pro
ENST00000578147.5:c.1753A>C ENSP00000463963.1:p.Thr585Pro
ENST00000581514.1:n.409A>C
NM_000334.4:c.1753A>C MANE Select NP_000325.4:p.Thr585Pro
XM_005257566.3:c.1753A>C XP_005257623.1:p.Thr585Pro
XR_934910.1:n.124+563T>G
XR_001752969.1:n.1276+563T>G
XR_934910.2:n.1276+563T>G