Canonical Allele Identifier: CA1772543565
Gene: ADRA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26866713A= , CM000670.2:g.26866713A= GRCh38
NC_000008.10:g.26724230A= , CM000670.1:g.26724230A= GRCh37
NC_000008.9:g.26780147A= NCBI36
NG_029395.1:g.3693T=

Transcript Alleles

HGVS Amino-acid change
ENST00000380573.4:c.-687+223T= MANE Select ENSP00000369947.3:n.-687+223T=
ENST00000380573.3:c.-687+223T= ENSP00000369947.3:n.-687+223T=
XM_005273414.3:c.-687+223T= XP_005273471.1:n.-687+223T=
XM_006716292.2:c.-687+223T= XP_006716355.1:n.-687+223T=
XM_006716293.2:c.-687+223T= XP_006716356.1:n.-687+223T=
XM_011544411.1:c.-687+223T= XP_011542713.1:n.-687+223T=
XM_011544412.1:c.-687+223T= XP_011542714.1:n.-687+223T=
NM_000680.3:c.-687+223T= NP_000671.2:n.-687+223T=
XM_006716292.3:c.-687+223T= XP_006716355.1:n.-687+223T=
XM_006716293.4:c.-687+223T= XP_006716356.1:n.-687+223T=
XM_011544411.2:c.-687+223T= XP_011542713.1:n.-687+223T=
XM_011544412.3:c.-687+223T= XP_011542714.1:n.-687+223T=
XM_017013094.1:c.-687+223T= XP_016868583.1:n.-687+223T=
XM_017013095.1:c.-687+223T= XP_016868584.1:n.-687+223T=
XM_017013096.1:c.-687+223T= XP_016868585.1:n.-687+223T=
XR_001745476.1:n.335+223T=
XR_001745477.1:n.335+223T=
NM_000680.4:c.-687+223T= MANE Select NP_000671.2:n.-687+223T=