Canonical Allele Identifier: CA2695226826
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941175_63941186del , CM000679.2:g.63941175_63941186del GRCh38
NC_000017.10:g.62018535_62018546del , CM000679.1:g.62018535_62018546del GRCh37
NC_000017.9:g.59372267_59372278del NCBI36
NG_011699.1:g.36736_36747del

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.5099_5110del MANE Select ENSP00000396320.1:p.Thr1700_Glu1703del
ENST00000578147.5:c.5099_5110del ENSP00000463963.1:p.Thr1700_Glu1703del
NM_000334.4:c.5099_5110del MANE Select NP_000325.4:p.Thr1700_Glu1703del
XM_005257566.3:c.5099_5110del XP_005257623.1:p.Thr1700_Glu1703del