Canonical Allele Identifier: CA8708802
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs754668970
ExAC: 17:62018393 G / A
gnomAD v2: 17-62018393-G-A
gnomAD v4: 17-63941033-G-A
MyVariant Identifiers: chr17:g.62018393G>A (hg19) chr17:g.63941033G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941033G>A , CM000679.2:g.63941033G>A GRCh38
NC_000017.10:g.62018393G>A , CM000679.1:g.62018393G>A GRCh37
NC_000017.9:g.59372125G>A NCBI36
NG_011699.1:g.36886C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.5249C>T MANE Select ENSP00000396320.1:p.Ala1750Val
ENST00000578147.5:c.5249C>T ENSP00000463963.1:p.Ala1750Val
NM_000334.4:c.5249C>T MANE Select NP_000325.4:p.Ala1750Val
XM_005257566.3:c.5249C>T XP_005257623.1:p.Ala1750Val
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