Canonical Allele Identifier: CA2603926736

Gene: ADCY5

Linked Data

• dbSNP Id: rs2108477067
• gnomAD v3: 3-123346887-CTGTATCGCTTCG-C
• gnomAD v4: 3-123346887-CTGTATCGCTTCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123346891_123346902del , CM000665.2:g.123346891_123346902del	GRCh38
NC_000003.11:g.123065738_123065749del , CM000665.1:g.123065738_123065749del	GRCh37
NC_000003.10:g.124548428_124548439del	NCBI36
NG_033882.1:g.106647_106658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.83+883_83+894del	ENSP00000420082.2:n.83+883_83+894del
ENST00000470367.2:c.371+883_371+894del	ENSP00000514541.1:n.371+883_371+894del
ENST00000483566.2:c.83+883_83+894del	ENSP00000420252.2:n.83+883_83+894del
ENST00000699714.1:c.83+883_83+894del	ENSP00000514539.1:n.83+883_83+894del
ENST00000699715.1:c.83+883_83+894del	ENSP00000514540.1:n.83+883_83+894del
ENST00000699716.1:c.83+883_83+894del	ENSP00000514542.1:n.83+883_83+894del
ENST00000699718.1:c.1406+883_1406+894del	ENSP00000514543.1:n.1406+883_1406+894del
ENST00000462833.6:c.1406+883_1406+894del MANE Select	ENSP00000419361.1:n.1406+883_1406+894del
ENST00000309879.9:c.356+883_356+894del	ENSP00000308685.5:n.356+883_356+894del
ENST00000462833.5:c.1406+883_1406+894del	ENSP00000419361.1:n.1406+883_1406+894del
ENST00000466617.5:c.83+883_83+894del	ENSP00000420082.1:n.83+883_83+894del
ENST00000476455.1:c.*73+883_*73+894del	ENSP00000417789.1:n.*73+883_*73+894del
ENST00000483566.1:c.83+883_83+894del	ENSP00000420252.1:n.83+883_83+894del
ENST00000491190.5:c.305+883_305+894del	ENSP00000418537.1:n.305+883_305+894del
NM_001199642.1:c.356+883_356+894del	NP_001186571.1:n.356+883_356+894del
NM_183357.2:c.1406+883_1406+894del	NP_899200.1:n.1406+883_1406+894del
XM_005247077.2:c.1406+883_1406+894del	XP_005247134.1:n.1406+883_1406+894del
XM_005247078.1:c.356+883_356+894del	XP_005247135.1:n.356+883_356+894del
XM_006713483.1:c.305+883_305+894del	XP_006713546.1:n.305+883_305+894del
XM_006713484.1:c.83+883_83+894del	XP_006713547.1:n.83+883_83+894del
XM_011512358.1:c.1406+883_1406+894del	XP_011510660.1:n.1406+883_1406+894del
XM_011512359.1:c.407+883_407+894del	XP_011510661.1:n.407+883_407+894del
XM_011512360.1:c.317+883_317+894del	XP_011510662.1:n.317+883_317+894del
XM_011512361.1:c.83+883_83+894del	XP_011510663.1:n.83+883_83+894del
XM_005247077.4:c.1406+883_1406+894del	XP_005247134.1:n.1406+883_1406+894del
XM_011512359.2:c.407+883_407+894del	XP_011510661.1:n.407+883_407+894del
XM_011512360.3:c.317+883_317+894del	XP_011510662.1:n.317+883_317+894del
XM_017005638.1:c.308+883_308+894del	XP_016861127.1:n.308+883_308+894del
XM_017005639.1:c.308+883_308+894del	XP_016861128.1:n.308+883_308+894del
NM_001378259.1:c.1406+883_1406+894del	NP_001365188.1:n.1406+883_1406+894del
NM_183357.3:c.1406+883_1406+894del MANE Select	NP_899200.1:n.1406+883_1406+894del