Canonical Allele Identifier: CA1053000735

Gene: ADCY5

Linked Data

• dbSNP Id: rs1938623385
• gnomAD v3: 3-123284811-TCTGACTGCCCAGCCCTGTTGCCGCCC-T
• gnomAD v4: 3-123284811-TCTGACTGCCCAGCCCTGTTGCCGCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284817_123284842del , CM000665.2:g.123284817_123284842del	GRCh38
NC_000003.11:g.123003664_123003689del , CM000665.1:g.123003664_123003689del	GRCh37
NC_000003.10:g.124486354_124486379del	NCBI36
NG_033882.1:g.168709_168734del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2335-101_2335-76del	ENSP00000420082.2:n.2335-101_2335-76del
ENST00000470367.2:c.2623-101_2623-76del	ENSP00000514541.1:n.2623-101_2623-76del
ENST00000483566.2:c.2335-101_2335-76del	ENSP00000420252.2:n.2335-101_2335-76del
ENST00000699714.1:c.2335-101_2335-76del	ENSP00000514539.1:n.2335-101_2335-76del
ENST00000699715.1:c.2335-101_2335-76del	ENSP00000514540.1:n.2335-101_2335-76del
ENST00000699716.1:c.2335-101_2335-76del	ENSP00000514542.1:n.2335-101_2335-76del
ENST00000699717.1:n.2061-101_2061-76del
ENST00000699718.1:c.3733-101_3733-76del	ENSP00000514543.1:n.3733-101_3733-76del
ENST00000462833.6:c.3658-101_3658-76del MANE Select	ENSP00000419361.1:n.3658-101_3658-76del
ENST00000309879.9:c.2608-101_2608-76del	ENSP00000308685.5:n.2608-101_2608-76del
ENST00000462833.5:c.3658-101_3658-76del	ENSP00000419361.1:n.3658-101_3658-76del
ENST00000478092.1:n.428-101_428-76del
ENST00000491190.5:c.2632-101_2632-76del	ENSP00000418537.1:n.2632-101_2632-76del
NM_001199642.1:c.2608-101_2608-76del	NP_001186571.1:n.2608-101_2608-76del
NM_183357.2:c.3658-101_3658-76del	NP_899200.1:n.3658-101_3658-76del
XM_005247077.2:c.3733-101_3733-76del	XP_005247134.1:n.3733-101_3733-76del
XM_005247078.1:c.2683-101_2683-76del	XP_005247135.1:n.2683-101_2683-76del
XM_006713483.1:c.2632-101_2632-76del	XP_006713546.1:n.2632-101_2632-76del
XM_006713484.1:c.2410-101_2410-76del	XP_006713547.1:n.2410-101_2410-76del
XM_011512359.1:c.2734-101_2734-76del	XP_011510661.1:n.2734-101_2734-76del
XM_011512360.1:c.2644-101_2644-76del	XP_011510662.1:n.2644-101_2644-76del
XM_011512361.1:c.2410-101_2410-76del	XP_011510663.1:n.2410-101_2410-76del
XM_005247077.4:c.3733-101_3733-76del	XP_005247134.1:n.3733-101_3733-76del
XM_011512359.2:c.2734-101_2734-76del	XP_011510661.1:n.2734-101_2734-76del
XM_011512360.3:c.2644-101_2644-76del	XP_011510662.1:n.2644-101_2644-76del
XM_017005638.1:c.2635-101_2635-76del	XP_016861127.1:n.2635-101_2635-76del
XM_017005639.1:c.2635-101_2635-76del	XP_016861128.1:n.2635-101_2635-76del
NM_001378259.1:c.3733-101_3733-76del	NP_001365188.1:n.3733-101_3733-76del
NM_183357.3:c.3658-101_3658-76del MANE Select	NP_899200.1:n.3658-101_3658-76del