Canonical Allele Identifier: CA2270163860
Gene: SCN4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63947257T= , CM000679.2:g.63947257T= GRCh38
NC_000017.10:g.62024617T= , CM000679.1:g.62024617T= GRCh37
NC_000017.9:g.59378349T= NCBI36
NG_011699.1:g.30662A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3319-90A= MANE Select ENSP00000396320.1:n.3319-90A=
ENST00000578147.5:c.3319-90A= ENSP00000463963.1:n.3319-90A=
NM_000334.4:c.3319-90A= MANE Select NP_000325.4:n.3319-90A=
XM_005257566.3:c.3319-90A= XP_005257623.1:n.3319-90A=