Canonical Allele Identifier: CA2639323194
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63968215_63968223del , CM000679.2:g.63968215_63968223del GRCh38
NC_000017.10:g.62045575_62045583del , CM000679.1:g.62045575_62045583del GRCh37
NC_000017.9:g.59399307_59399315del NCBI36
NG_011699.1:g.9696_9704del

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.836_844del MANE Select ENSP00000396320.1:p.Lys279_Arg282delinsSer
ENST00000578147.5:c.836_844del ENSP00000463963.1:p.Lys279_Arg282delinsSer
NM_000334.4:c.836_844del MANE Select NP_000325.4:p.Lys279_Arg282delinsSer
XM_005257566.3:c.836_844del XP_005257623.1:p.Lys279_Arg282delinsSer