Canonical Allele Identifier: CA400616576
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942945A>T , CM000679.2:g.63942945A>T GRCh38
NC_000017.10:g.62020305A>T , CM000679.1:g.62020305A>T GRCh37
NC_000017.9:g.59374037A>T NCBI36
NG_011699.1:g.34974T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.4169T>A MANE Select ENSP00000396320.1:p.Met1390Lys
ENST00000578147.5:c.4169T>A ENSP00000463963.1:p.Met1390Lys
NM_000334.4:c.4169T>A MANE Select NP_000325.4:p.Met1390Lys
XM_005257566.3:c.4169T>A XP_005257623.1:p.Met1390Lys