Canonical Allele Identifier: CA1772541642
Gene: ADRA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26865444C= , CM000670.2:g.26865444C= GRCh38
NC_000008.10:g.26722961C= , CM000670.1:g.26722961C= GRCh37
NC_000008.9:g.26778878C= NCBI36
NG_029395.1:g.4962G=

Transcript Alleles

HGVS Amino-acid change
ENST00000380573.4:c.-475G= MANE Select ENSP00000369947.3:n.-475G=
ENST00000380573.3:c.-475G= ENSP00000369947.3:n.-475G=
XM_005273414.3:c.-475G= XP_005273471.1:n.-475G=
XM_006716292.2:c.-475G= XP_006716355.1:n.-475G=
XM_006716293.2:c.-475G= XP_006716356.1:n.-475G=
XM_011544411.1:c.-475G= XP_011542713.1:n.-475G=
XM_011544412.1:c.-475G= XP_011542714.1:n.-475G=
NM_000680.3:c.-475G= NP_000671.2:n.-475G=
NM_001322502.1:c.-475G= NP_001309431.1:n.-475G=
NM_001322503.1:c.-475G= NP_001309432.1:n.-475G=
NM_001322504.1:c.-475G= NP_001309433.1:n.-475G=
NM_033302.3:c.-475G= NP_150645.2:n.-475G=
NM_033303.4:c.-475G= NP_150646.3:n.-475G=
NM_033304.3:c.-475G= NP_150647.2:n.-475G=
NR_136343.1:n.212G=
XM_006716292.3:c.-475G= XP_006716355.1:n.-475G=
XM_006716293.4:c.-475G= XP_006716356.1:n.-475G=
XM_011544411.2:c.-475G= XP_011542713.1:n.-475G=
XM_011544412.3:c.-475G= XP_011542714.1:n.-475G=
XM_017013094.1:c.-475G= XP_016868583.1:n.-475G=
XM_017013095.1:c.-475G= XP_016868584.1:n.-475G=
XM_017013096.1:c.-475G= XP_016868585.1:n.-475G=
XR_001745476.1:n.547G=
XR_001745477.1:n.547G=
NM_000680.4:c.-475G= MANE Select NP_000671.2:n.-475G=