Canonical Allele Identifier: CA12877444
Gene: ADRA1A HGNC NCBI

Linked Data

dbSNP Id: rs573542

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26866301C>T , CM000670.2:g.26866301C>T GRCh38
NC_000008.10:g.26723818C>T , CM000670.1:g.26723818C>T GRCh37
NC_000008.9:g.26779735C>T NCBI36
NG_029395.1:g.4105G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380573.4:c.-687+635G>A MANE Select ENSP00000369947.3:n.-687+635G>A
ENST00000380573.3:c.-687+635G>A ENSP00000369947.3:n.-687+635G>A
XM_005273414.3:c.-687+635G>A XP_005273471.1:n.-687+635G>A
XM_006716292.2:c.-687+635G>A XP_006716355.1:n.-687+635G>A
XM_006716293.2:c.-687+635G>A XP_006716356.1:n.-687+635G>A
XM_011544411.1:c.-687+635G>A XP_011542713.1:n.-687+635G>A
XM_011544412.1:c.-687+635G>A XP_011542714.1:n.-687+635G>A
NM_000680.3:c.-687+635G>A NP_000671.2:n.-687+635G>A
XM_006716292.3:c.-687+635G>A XP_006716355.1:n.-687+635G>A
XM_006716293.4:c.-687+635G>A XP_006716356.1:n.-687+635G>A
XM_011544411.2:c.-687+635G>A XP_011542713.1:n.-687+635G>A
XM_011544412.3:c.-687+635G>A XP_011542714.1:n.-687+635G>A
XM_017013094.1:c.-687+635G>A XP_016868583.1:n.-687+635G>A
XM_017013095.1:c.-687+635G>A XP_016868584.1:n.-687+635G>A
XM_017013096.1:c.-687+635G>A XP_016868585.1:n.-687+635G>A
XR_001745476.1:n.335+635G>A
XR_001745477.1:n.335+635G>A
NM_000680.4:c.-687+635G>A MANE Select NP_000671.2:n.-687+635G>A