Canonical Allele Identifier: CA2346946119
Gene: ADRA1D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234764T= , CM000682.2:g.4234764T= GRCh38
NC_000020.10:g.4215411T= , CM000682.1:g.4215411T= GRCh37
NC_000020.9:g.4163411T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12634A= MANE Select ENSP00000368766.4:n.1112-12634A=
ENST00000379453.5:c.1112-12634A= ENSP00000368766.4:n.1112-12634A=
NM_000678.3:c.1112-12634A= NP_000669.1:n.1112-12634A=
NM_000678.4:c.1112-12634A= MANE Select NP_000669.1:n.1112-12634A=