Canonical Allele Identifier: CA400617240
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs1317823192
gnomAD v2: 17-62022046-T-A
MyVariant Identifiers: chr17:g.62022046T>A (hg19) chr17:g.63944686T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63944686T>A , CM000679.2:g.63944686T>A GRCh38
NC_000017.10:g.62022046T>A , CM000679.1:g.62022046T>A GRCh37
NC_000017.9:g.59375778T>A NCBI36
NG_011699.1:g.33233A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3899A>T MANE Select ENSP00000396320.1:p.Gln1300Leu
ENST00000578147.5:c.3899A>T ENSP00000463963.1:p.Gln1300Leu
NM_000334.4:c.3899A>T MANE Select NP_000325.4:p.Gln1300Leu
XM_005257566.3:c.3899A>T XP_005257623.1:p.Gln1300Leu
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