Canonical Allele Identifier: CA2639309749
Gene: SCN4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63944628del , CM000679.2:g.63944628del GRCh38
NC_000017.10:g.62021988del , CM000679.1:g.62021988del GRCh37
NC_000017.9:g.59375720del NCBI36
NG_011699.1:g.33293del

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.3912+47del MANE Select ENSP00000396320.1:n.3912+47del
ENST00000578147.5:c.3916+43del ENSP00000463963.1:n.3916+43del
NM_000334.4:c.3912+47del MANE Select NP_000325.4:n.3912+47del
XM_005257566.3:c.3912+47del XP_005257623.1:n.3912+47del