Canonical Allele Identifier: CA2270161342
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942240C= , CM000679.2:g.63942240C= GRCh38
NC_000017.10:g.62019600C= , CM000679.1:g.62019600C= GRCh37
NC_000017.9:g.59373332C= NCBI36
NG_011699.1:g.35679G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.4289-247G= MANE Select ENSP00000396320.1:n.4289-247G=
ENST00000578147.5:c.4289-247G= ENSP00000463963.1:n.4289-247G=
NM_000334.4:c.4289-247G= MANE Select NP_000325.4:n.4289-247G=
XM_005257566.3:c.4289-247G= XP_005257623.1:n.4289-247G=