Canonical Allele Identifier: CA915950729
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 651872
ClinVar RCV Id: RCV000807307
dbSNP Id: rs1598404848

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941172_63941174del , CM000679.2:g.63941172_63941174del GRCh38
NC_000017.10:g.62018532_62018534del , CM000679.1:g.62018532_62018534del GRCh37
NC_000017.9:g.59372264_59372266del NCBI36
NG_011699.1:g.36747_36749del

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.5110_5112del MANE Select ENSP00000396320.1:p.Lys1704del
ENST00000578147.5:c.5110_5112del ENSP00000463963.1:p.Lys1704del
NM_000334.4:c.5110_5112del MANE Select NP_000325.4:p.Lys1704del
XM_005257566.3:c.5110_5112del XP_005257623.1:p.Lys1704del