Canonical Allele Identifier: CA8709760
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1985095
ClinVar RCV Id: RCV002780534 RCV003491150
dbSNP Id: rs371523329
ExAC: 17:62038710 G / A
gnomAD v2: 17-62038710-G-A
gnomAD v3: 17-63961350-G-A
gnomAD v4: 17-63961350-G-A
MyVariant Identifiers: chr17:g.62038710G>A (hg19) chr17:g.63961350G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63961350G>A , CM000679.2:g.63961350G>A GRCh38
NC_000017.10:g.62038710G>A , CM000679.1:g.62038710G>A GRCh37
NC_000017.9:g.59392442G>A NCBI36
NG_011699.1:g.16569C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.1688C>T MANE Select ENSP00000396320.1:p.Pro563Leu
ENST00000578147.5:c.1688C>T ENSP00000463963.1:p.Pro563Leu
ENST00000581514.1:n.344C>T
NM_000334.4:c.1688C>T MANE Select NP_000325.4:p.Pro563Leu
XM_005257566.3:c.1688C>T XP_005257623.1:p.Pro563Leu
XR_934910.1:n.124+628G>A
XR_001752969.1:n.1276+628G>A
XR_934910.2:n.1276+628G>A
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