Canonical Allele Identifier: CA2346946232
Gene: ADRA1D HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234983C= , CM000682.2:g.4234983C= GRCh38
NC_000020.10:g.4215630C= , CM000682.1:g.4215630C= GRCh37
NC_000020.9:g.4163630C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12853G= MANE Select ENSP00000368766.4:n.1112-12853G=
ENST00000379453.5:c.1112-12853G= ENSP00000368766.4:n.1112-12853G=
NM_000678.3:c.1112-12853G= NP_000669.1:n.1112-12853G=
NM_000678.4:c.1112-12853G= MANE Select NP_000669.1:n.1112-12853G=
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