Canonical Allele Identifier: CA2639308428
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942937_63942939del , CM000679.2:g.63942937_63942939del GRCh38
NC_000017.10:g.62020297_62020299del , CM000679.1:g.62020297_62020299del GRCh37
NC_000017.9:g.59374029_59374031del NCBI36
NG_011699.1:g.34988_34990del

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.4183_4185del MANE Select ENSP00000396320.1:p.Ile1395del
ENST00000578147.5:c.4183_4185del ENSP00000463963.1:p.Ile1395del
NM_000334.4:c.4183_4185del MANE Select NP_000325.4:p.Ile1395del
XM_005257566.3:c.4183_4185del XP_005257623.1:p.Ile1395del