Canonical Allele Identifier: CA2346946241
Gene: ADRA1D HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4235020T= , CM000682.2:g.4235020T= GRCh38
NC_000020.10:g.4215667T= , CM000682.1:g.4215667T= GRCh37
NC_000020.9:g.4163667T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1111+12827A= MANE Select ENSP00000368766.4:n.1111+12827A=
ENST00000379453.5:c.1111+12827A= ENSP00000368766.4:n.1111+12827A=
NM_000678.3:c.1111+12827A= NP_000669.1:n.1111+12827A=
NM_000678.4:c.1111+12827A= MANE Select NP_000669.1:n.1111+12827A=
Search 100 bp 5'
Search 100 bp 3'