Canonical Allele Identifier: CA2667292490

Gene: ADCY5

Linked Data

• gnomAD v4: 3-123284845-AGAAGGAGAGGGGCAGCTGCCCCACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284848_123284872del , CM000665.2:g.123284848_123284872del	GRCh38
NC_000003.11:g.123003695_123003719del , CM000665.1:g.123003695_123003719del	GRCh37
NC_000003.10:g.124486385_124486409del	NCBI36
NG_033882.1:g.168676_168700del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2335-134_2335-110del	ENSP00000420082.2:n.2335-134_2335-110del
ENST00000470367.2:c.2623-134_2623-110del	ENSP00000514541.1:n.2623-134_2623-110del
ENST00000483566.2:c.2335-134_2335-110del	ENSP00000420252.2:n.2335-134_2335-110del
ENST00000699714.1:c.2335-134_2335-110del	ENSP00000514539.1:n.2335-134_2335-110del
ENST00000699715.1:c.2335-134_2335-110del	ENSP00000514540.1:n.2335-134_2335-110del
ENST00000699716.1:c.2335-134_2335-110del	ENSP00000514542.1:n.2335-134_2335-110del
ENST00000699717.1:n.2061-134_2061-110del
ENST00000699718.1:c.3733-134_3733-110del	ENSP00000514543.1:n.3733-134_3733-110del
ENST00000462833.6:c.3658-134_3658-110del MANE Select	ENSP00000419361.1:n.3658-134_3658-110del
ENST00000309879.9:c.2608-134_2608-110del	ENSP00000308685.5:n.2608-134_2608-110del
ENST00000462833.5:c.3658-134_3658-110del	ENSP00000419361.1:n.3658-134_3658-110del
ENST00000478092.1:n.428-134_428-110del
ENST00000491190.5:c.2632-134_2632-110del	ENSP00000418537.1:n.2632-134_2632-110del
NM_001199642.1:c.2608-134_2608-110del	NP_001186571.1:n.2608-134_2608-110del
NM_183357.2:c.3658-134_3658-110del	NP_899200.1:n.3658-134_3658-110del
XM_005247077.2:c.3733-134_3733-110del	XP_005247134.1:n.3733-134_3733-110del
XM_005247078.1:c.2683-134_2683-110del	XP_005247135.1:n.2683-134_2683-110del
XM_006713483.1:c.2632-134_2632-110del	XP_006713546.1:n.2632-134_2632-110del
XM_006713484.1:c.2410-134_2410-110del	XP_006713547.1:n.2410-134_2410-110del
XM_011512359.1:c.2734-134_2734-110del	XP_011510661.1:n.2734-134_2734-110del
XM_011512360.1:c.2644-134_2644-110del	XP_011510662.1:n.2644-134_2644-110del
XM_011512361.1:c.2410-134_2410-110del	XP_011510663.1:n.2410-134_2410-110del
XM_005247077.4:c.3733-134_3733-110del	XP_005247134.1:n.3733-134_3733-110del
XM_011512359.2:c.2734-134_2734-110del	XP_011510661.1:n.2734-134_2734-110del
XM_011512360.3:c.2644-134_2644-110del	XP_011510662.1:n.2644-134_2644-110del
XM_017005638.1:c.2635-134_2635-110del	XP_016861127.1:n.2635-134_2635-110del
XM_017005639.1:c.2635-134_2635-110del	XP_016861128.1:n.2635-134_2635-110del
NM_001378259.1:c.3733-134_3733-110del	NP_001365188.1:n.3733-134_3733-110del
NM_183357.3:c.3658-134_3658-110del MANE Select	NP_899200.1:n.3658-134_3658-110del