Canonical Allele Identifier: CA400616560
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1028201
ClinVar RCV Id: RCV001329190
dbSNP Id: rs1908590856
MyVariant Identifiers: chr17:g.62020299A>G (hg19) chr17:g.63942939A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942939A>G , CM000679.2:g.63942939A>G GRCh38
NC_000017.10:g.62020299A>G , CM000679.1:g.62020299A>G GRCh37
NC_000017.9:g.59374031A>G NCBI36
NG_011699.1:g.34980T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.4175T>C MANE Select ENSP00000396320.1:p.Phe1392Ser
ENST00000578147.5:c.4175T>C ENSP00000463963.1:p.Phe1392Ser
NM_000334.4:c.4175T>C MANE Select NP_000325.4:p.Phe1392Ser
XM_005257566.3:c.4175T>C XP_005257623.1:p.Phe1392Ser
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