Canonical Allele Identifier: CA657451051
Gene: ADRA1D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234750T>C , CM000682.2:g.4234750T>C GRCh38
NC_000020.10:g.4215397T>C , CM000682.1:g.4215397T>C GRCh37
NC_000020.9:g.4163397T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12620A>G MANE Select ENSP00000368766.4:n.1112-12620A>G
ENST00000379453.5:c.1112-12620A>G ENSP00000368766.4:n.1112-12620A>G
NM_000678.3:c.1112-12620A>G NP_000669.1:n.1112-12620A>G
NM_000678.4:c.1112-12620A>G MANE Select NP_000669.1:n.1112-12620A>G