Canonical Allele Identifier: CA8708797
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs373278632

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941018C>G , CM000679.2:g.63941018C>G GRCh38
NC_000017.10:g.62018378C>G , CM000679.1:g.62018378C>G GRCh37
NC_000017.9:g.59372110C>G NCBI36
NG_011699.1:g.36901G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.5264G>C MANE Select ENSP00000396320.1:p.Arg1755Pro
ENST00000578147.5:c.5264G>C ENSP00000463963.1:p.Arg1755Pro
NM_000334.4:c.5264G>C MANE Select NP_000325.4:p.Arg1755Pro
XM_005257566.3:c.5264G>C XP_005257623.1:p.Arg1755Pro