Canonical Allele Identifier: CA8709024
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs755789100

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942837A>G , CM000679.2:g.63942837A>G GRCh38
NC_000017.10:g.62020197A>G , CM000679.1:g.62020197A>G GRCh37
NC_000017.9:g.59373929A>G NCBI36
NG_011699.1:g.35082T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.4277T>C MANE Select ENSP00000396320.1:p.Leu1426Pro
ENST00000578147.5:c.4277T>C ENSP00000463963.1:p.Leu1426Pro
NM_000334.4:c.4277T>C MANE Select NP_000325.4:p.Leu1426Pro
XM_005257566.3:c.4277T>C XP_005257623.1:p.Leu1426Pro