Canonical Allele Identifier: CA2639323054
Gene: SCN4A HGNC NCBI

Linked Data

gnomAD v4: 17-63941249-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941251del , CM000679.2:g.63941251del GRCh38
NC_000017.10:g.62018611del , CM000679.1:g.62018611del GRCh37
NC_000017.9:g.59372343del NCBI36
NG_011699.1:g.36669del

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.5032del MANE Select ENSP00000396320.1:p.Asp1678ThrfsTer6
ENST00000578147.5:c.5032del ENSP00000463963.1:p.Asp1678ThrfsTer6
NM_000334.4:c.5032del MANE Select NP_000325.4:p.Asp1678ThrfsTer6
XM_005257566.3:c.5032del XP_005257623.1:p.Asp1678ThrfsTer6
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