Canonical Allele Identifier: CA4687163
Gene: ADRA1A HGNC NCBI

Linked Data

dbSNP Id: rs757286802
gnomAD v2: 8-26721793-C-A
gnomAD v4: 8-26864276-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26864276C>A , CM000670.2:g.26864276C>A GRCh38
NC_000008.10:g.26721793C>A , CM000670.1:g.26721793C>A GRCh37
NC_000008.9:g.26777710C>A NCBI36
NG_029395.1:g.6130G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380573.4:c.694G>T MANE Select ENSP00000369947.3:p.Val232Leu
ENST00000276393.8:c.694G>T ENSP00000276393.4:p.Val232Leu
ENST00000354550.4:c.694G>T ENSP00000346557.4:p.Val232Leu
ENST00000380572.3:c.694G>T ENSP00000369946.3:p.Val232Leu
ENST00000380573.3:c.694G>T ENSP00000369947.3:p.Val232Leu
ENST00000380582.7:c.694G>T ENSP00000369956.3:p.Val232Leu
ENST00000380586.5:c.694G>T ENSP00000369960.1:p.Val232Leu
ENST00000519096.5:c.694G>T ENSP00000431073.1:p.Val232Leu
ENST00000519229.5:c.694G>T ENSP00000430793.1:p.Val232Leu
ENST00000521711.5:c.694G>T ENSP00000430414.1:p.Val232Leu
NM_000680.2:c.694G>T NP_000671.2:p.Val232Leu
NM_033302.2:c.694G>T NP_150645.2:p.Val232Leu
NM_033303.3:c.694G>T NP_150646.3:p.Val232Leu
NM_033304.2:c.694G>T NP_150647.2:p.Val232Leu
XM_005273414.3:c.694G>T XP_005273471.1:p.Val232Leu
XM_006716292.2:c.694G>T XP_006716355.1:p.Val232Leu
XM_006716293.2:c.694G>T XP_006716356.1:p.Val232Leu
XM_011544411.1:c.694G>T XP_011542713.1:p.Val232Leu
XM_011544412.1:c.694G>T XP_011542714.1:p.Val232Leu
NM_000680.3:c.694G>T NP_000671.2:p.Val232Leu
NM_001322502.1:c.694G>T NP_001309431.1:p.Val232Leu
NM_001322503.1:c.694G>T NP_001309432.1:p.Val232Leu
NM_001322504.1:c.694G>T NP_001309433.1:p.Val232Leu
NM_033302.3:c.694G>T NP_150645.2:p.Val232Leu
NM_033303.4:c.694G>T NP_150646.3:p.Val232Leu
NM_033304.3:c.694G>T NP_150647.2:p.Val232Leu
NR_136343.1:n.1380G>T
XM_006716292.3:c.694G>T XP_006716355.1:p.Val232Leu
XM_006716293.4:c.694G>T XP_006716356.1:p.Val232Leu
XM_011544411.2:c.694G>T XP_011542713.1:p.Val232Leu
XM_011544412.3:c.694G>T XP_011542714.1:p.Val232Leu
XM_017013094.1:c.694G>T XP_016868583.1:p.Val232Leu
XM_017013095.1:c.694G>T XP_016868584.1:p.Val232Leu
XM_017013096.1:c.694G>T XP_016868585.1:p.Val232Leu
XR_001745476.1:n.1715G>T
XR_001745477.1:n.1715G>T
NM_000680.4:c.694G>T MANE Select NP_000671.2:p.Val232Leu