Canonical Allele Identifier: CA400617473
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 477419
ClinVar RCV Id: RCV000541828 RCV002506373
dbSNP Id: rs1398605254
gnomAD v2: 17-62022149-C-T
gnomAD v3: 17-63944789-C-T
gnomAD v4: 17-63944789-C-T
MyVariant Identifiers: chr17:g.62022149C>T (hg19) chr17:g.63944789C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63944789C>T , CM000679.2:g.63944789C>T GRCh38
NC_000017.10:g.62022149C>T , CM000679.1:g.62022149C>T GRCh37
NC_000017.9:g.59375881C>T NCBI36
NG_011699.1:g.33130G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3796G>A MANE Select ENSP00000396320.1:p.Glu1266Lys
ENST00000578147.5:c.3796G>A ENSP00000463963.1:p.Glu1266Lys
NM_000334.4:c.3796G>A MANE Select NP_000325.4:p.Glu1266Lys
XM_005257566.3:c.3796G>A XP_005257623.1:p.Glu1266Lys
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