Canonical Allele Identifier: CA1772541698

Gene: ADRA1A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.26865476_26865499delinsGTTGGGTAGCGCAGCGCTACAGGT , CM000670.2:g.26865476_26865499delinsGTTGGGTAGCGCAGCGCTACAGGT	GRCh38
NC_000008.10:g.26722993_26723016delinsGTTGGGTAGCGCAGCGCTACAGGT , CM000670.1:g.26722993_26723016delinsGTTGGGTAGCGCAGCGCTACAGGT	GRCh37
NC_000008.9:g.26778910_26778933delinsGTTGGGTAGCGCAGCGCTACAGGT	NCBI36
NG_029395.1:g.4907_4930delinsACCTGTAGCGCTGCGCTACCCAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380573.4:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC MANE Select	ENSP00000369947.3:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
ENST00000380573.3:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	ENSP00000369947.3:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_005273414.3:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_005273471.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_006716292.2:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_006716355.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_006716293.2:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_006716356.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_011544411.1:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_011542713.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_011544412.1:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_011542714.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
NM_000680.3:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	NP_000671.2:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
NM_001322502.1:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	NP_001309431.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
NM_001322503.1:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	NP_001309432.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
NM_001322504.1:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	NP_001309433.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
NM_033302.3:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	NP_150645.2:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
NM_033303.4:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	NP_150646.3:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
NM_033304.3:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	NP_150647.2:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
NR_136343.1:n.157_180delinsACCTGTAGCGCTGCGCTACCCAAC
XM_006716292.3:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_006716355.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_006716293.4:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_006716356.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_011544411.2:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_011542713.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_011544412.3:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_011542714.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_017013094.1:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_016868583.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_017013095.1:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_016868584.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XM_017013096.1:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC	XP_016868585.1:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC
XR_001745476.1:n.492_515delinsACCTGTAGCGCTGCGCTACCCAAC
XR_001745477.1:n.492_515delinsACCTGTAGCGCTGCGCTACCCAAC
NM_000680.4:c.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC MANE Select	NP_000671.2:n.-530_-507delinsACCTGTAGCGCTGCGCTACCCAAC