Canonical Allele Identifier: CA2270162487
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63944461C= , CM000679.2:g.63944461C= GRCh38
NC_000017.10:g.62021821C= , CM000679.1:g.62021821C= GRCh37
NC_000017.9:g.59375553C= NCBI36
NG_011699.1:g.33458G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3912+212G= MANE Select ENSP00000396320.1:n.3912+212G=
ENST00000578147.5:c.3916+208G= ENSP00000463963.1:n.3916+208G=
NM_000334.4:c.3912+212G= MANE Select NP_000325.4:n.3912+212G=
XM_005257566.3:c.3912+212G= XP_005257623.1:n.3912+212G=