Canonical Allele Identifier: CA1112092209
Gene: ADRA1A HGNC NCBI

Linked Data

dbSNP Id: rs1813933672
gnomAD v4: 8-26866790-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26866790C>A , CM000670.2:g.26866790C>A GRCh38
NC_000008.10:g.26724307C>A , CM000670.1:g.26724307C>A GRCh37
NC_000008.9:g.26780224C>A NCBI36
NG_029395.1:g.3616G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000380573.4:c.-687+146G>T MANE Select ENSP00000369947.3:n.-687+146G>T
ENST00000380573.3:c.-687+146G>T ENSP00000369947.3:n.-687+146G>T
XM_005273414.3:c.-687+146G>T XP_005273471.1:n.-687+146G>T
XM_006716292.2:c.-687+146G>T XP_006716355.1:n.-687+146G>T
XM_006716293.2:c.-687+146G>T XP_006716356.1:n.-687+146G>T
XM_011544411.1:c.-687+146G>T XP_011542713.1:n.-687+146G>T
XM_011544412.1:c.-687+146G>T XP_011542714.1:n.-687+146G>T
NM_000680.3:c.-687+146G>T NP_000671.2:n.-687+146G>T
XM_006716292.3:c.-687+146G>T XP_006716355.1:n.-687+146G>T
XM_006716293.4:c.-687+146G>T XP_006716356.1:n.-687+146G>T
XM_011544411.2:c.-687+146G>T XP_011542713.1:n.-687+146G>T
XM_011544412.3:c.-687+146G>T XP_011542714.1:n.-687+146G>T
XM_017013094.1:c.-687+146G>T XP_016868583.1:n.-687+146G>T
XM_017013095.1:c.-687+146G>T XP_016868584.1:n.-687+146G>T
XM_017013096.1:c.-687+146G>T XP_016868585.1:n.-687+146G>T
XR_001745476.1:n.335+146G>T
XR_001745477.1:n.335+146G>T
NM_000680.4:c.-687+146G>T MANE Select NP_000671.2:n.-687+146G>T