Canonical Allele Identifier: CA2346946114
Gene: ADRA1D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234755C= , CM000682.2:g.4234755C= GRCh38
NC_000020.10:g.4215402C= , CM000682.1:g.4215402C= GRCh37
NC_000020.9:g.4163402C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12625G= MANE Select ENSP00000368766.4:n.1112-12625G=
ENST00000379453.5:c.1112-12625G= ENSP00000368766.4:n.1112-12625G=
NM_000678.3:c.1112-12625G= NP_000669.1:n.1112-12625G=
NM_000678.4:c.1112-12625G= MANE Select NP_000669.1:n.1112-12625G=