Canonical Allele Identifier: CA2270161353
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942259G= , CM000679.2:g.63942259G= GRCh38
NC_000017.10:g.62019619G= , CM000679.1:g.62019619G= GRCh37
NC_000017.9:g.59373351G= NCBI36
NG_011699.1:g.35660C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.4289-266C= MANE Select ENSP00000396320.1:n.4289-266C=
ENST00000578147.5:c.4289-266C= ENSP00000463963.1:n.4289-266C=
NM_000334.4:c.4289-266C= MANE Select NP_000325.4:n.4289-266C=
XM_005257566.3:c.4289-266C= XP_005257623.1:n.4289-266C=