Canonical Allele Identifier: CA1772542801
Gene: ADRA1A HGNC NCBI

Linked Data

dbSNP Id: rs573542

Genomic Alleles

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

Transcript Alleles

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