Canonical Allele Identifier: CA8708955
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1162135
ClinVar RCV Id: RCV001506910
dbSNP Id: rs377064207
ExAC: 17:62019178 G / A
gnomAD v2: 17-62019178-G-A
MyVariant Identifiers: chr17:g.62019178G>A (hg19) chr17:g.63941818G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941818G>A , CM000679.2:g.63941818G>A GRCh38
NC_000017.10:g.62019178G>A , CM000679.1:g.62019178G>A GRCh37
NC_000017.9:g.59372910G>A NCBI36
NG_011699.1:g.36101C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.4464C>T MANE Select ENSP00000396320.1:p.Leu1488=
ENST00000578147.5:c.4464C>T ENSP00000463963.1:p.Leu1488=
NM_000334.4:c.4464C>T MANE Select NP_000325.4:p.Leu1488=
XM_005257566.3:c.4464C>T XP_005257623.1:p.Leu1488=
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