Canonical Allele Identifier: CA400617442
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63944776T>A , CM000679.2:g.63944776T>A GRCh38
NC_000017.10:g.62022136T>A , CM000679.1:g.62022136T>A GRCh37
NC_000017.9:g.59375868T>A NCBI36
NG_011699.1:g.33143A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3809A>T MANE Select ENSP00000396320.1:p.Tyr1270Phe
ENST00000578147.5:c.3809A>T ENSP00000463963.1:p.Tyr1270Phe
NM_000334.4:c.3809A>T MANE Select NP_000325.4:p.Tyr1270Phe
XM_005257566.3:c.3809A>T XP_005257623.1:p.Tyr1270Phe