Canonical Allele Identifier: CA15544391

Gene: ADRA1A

Linked Data

• dbSNP Id: rs13278849
• gnomAD v2: 8-26714874-G-A
• gnomAD v3: 8-26857357-G-A
• gnomAD v4: 8-26857357-G-A
• MyVariant Identifiers: chr8:g.26714874G>A (hg19) ; chr8:g.26857357G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.26857357G>A , CM000670.2:g.26857357G>A	GRCh38
NC_000008.10:g.26714874G>A , CM000670.1:g.26714874G>A	GRCh37
NC_000008.9:g.26770791G>A	NCBI36
NG_029395.1:g.13049C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000380573.4:c.883+6730C>T MANE Select	ENSP00000369947.3:n.883+6730C>T
ENST00000276393.8:c.883+6730C>T	ENSP00000276393.4:n.883+6730C>T
ENST00000354550.4:c.883+6730C>T	ENSP00000346557.4:n.883+6730C>T
ENST00000380572.3:c.883+6730C>T	ENSP00000369946.3:n.883+6730C>T
ENST00000380573.3:c.883+6730C>T	ENSP00000369947.3:n.883+6730C>T
ENST00000380582.7:c.883+6730C>T	ENSP00000369956.3:n.883+6730C>T
ENST00000380586.5:c.883+6730C>T	ENSP00000369960.1:n.883+6730C>T
ENST00000519096.5:c.*82+1675C>T	ENSP00000431073.1:n.*82+1675C>T
ENST00000519229.5:c.883+6730C>T	ENSP00000430793.1:n.883+6730C>T
ENST00000521711.5:c.*82+1675C>T	ENSP00000430414.1:n.*82+1675C>T
NM_000680.2:c.883+6730C>T	NP_000671.2:n.883+6730C>T
NM_033302.2:c.883+6730C>T	NP_150645.2:n.883+6730C>T
NM_033303.3:c.883+6730C>T	NP_150646.3:n.883+6730C>T
NM_033304.2:c.883+6730C>T	NP_150647.2:n.883+6730C>T
XM_005273414.3:c.883+6730C>T	XP_005273471.1:n.883+6730C>T
XM_006716292.2:c.883+6730C>T	XP_006716355.1:n.883+6730C>T
XM_006716293.2:c.883+6730C>T	XP_006716356.1:n.883+6730C>T
XM_011544412.1:c.883+6730C>T	XP_011542714.1:n.883+6730C>T
XR_949604.1:n.540-997G>A
NM_000680.3:c.883+6730C>T	NP_000671.2:n.883+6730C>T
NM_001322502.1:c.883+6730C>T	NP_001309431.1:n.883+6730C>T
NM_001322503.1:c.883+6730C>T	NP_001309432.1:n.883+6730C>T
NM_001322504.1:c.883+6730C>T	NP_001309433.1:n.883+6730C>T
NM_033302.3:c.883+6730C>T	NP_150645.2:n.883+6730C>T
NM_033303.4:c.883+6730C>T	NP_150646.3:n.883+6730C>T
NM_033304.3:c.883+6730C>T	NP_150647.2:n.883+6730C>T
NR_136343.1:n.1743+1675C>T
XM_006716292.3:c.883+6730C>T	XP_006716355.1:n.883+6730C>T
XM_006716293.4:c.883+6730C>T	XP_006716356.1:n.883+6730C>T
XM_011544412.3:c.883+6730C>T	XP_011542714.1:n.883+6730C>T
XM_017013094.1:c.883+6730C>T	XP_016868583.1:n.883+6730C>T
XM_017013095.1:c.883+6730C>T	XP_016868584.1:n.883+6730C>T
XM_017013096.1:c.883+6730C>T	XP_016868585.1:n.883+6730C>T
XR_001745476.1:n.2078+1675C>T
XR_001745477.1:n.1904+6730C>T
NM_000680.4:c.883+6730C>T MANE Select	NP_000671.2:n.883+6730C>T