Canonical Allele Identifier: CA1052997537

Gene: ADCY5

Linked Data

• gnomAD v3: 3-123377929-C-CAAAAAAAAAA
• gnomAD v4: 3-123377929-C-CAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123377939_123377948dup , CM000665.2:g.123377939_123377948dup	GRCh38
NC_000003.11:g.123096786_123096795dup , CM000665.1:g.123096786_123096795dup	GRCh37
NC_000003.10:g.124579476_124579485dup	NCBI36
NG_033882.1:g.75607_75616dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.-189-25358_-189-25349dup	ENSP00000420082.2:n.-189-25358_-189-25349dup
ENST00000470367.2:c.100-25358_100-25349dup	ENSP00000514541.1:n.100-25358_100-25349dup
ENST00000483566.2:c.-189-25358_-189-25349dup	ENSP00000420252.2:n.-189-25358_-189-25349dup
ENST00000699714.1:c.-189-25358_-189-25349dup	ENSP00000514539.1:n.-189-25358_-189-25349dup
ENST00000699715.1:c.-189-25358_-189-25349dup	ENSP00000514540.1:n.-189-25358_-189-25349dup
ENST00000699716.1:c.-189-25358_-189-25349dup	ENSP00000514542.1:n.-189-25358_-189-25349dup
ENST00000699718.1:c.1135-25358_1135-25349dup	ENSP00000514543.1:n.1135-25358_1135-25349dup
ENST00000462833.6:c.1135-25358_1135-25349dup MANE Select	ENSP00000419361.1:n.1135-25358_1135-25349dup
ENST00000309879.9:c.85-25358_85-25349dup	ENSP00000308685.5:n.85-25358_85-25349dup
ENST00000462833.5:c.1135-25358_1135-25349dup	ENSP00000419361.1:n.1135-25358_1135-25349dup
ENST00000466617.5:c.-189-25358_-189-25349dup	ENSP00000420082.1:n.-189-25358_-189-25349dup
ENST00000470367.1:n.430-25358_430-25349dup
ENST00000476455.1:c.-109-9893_-109-9884dup	ENSP00000417789.1:n.-109-9893_-109-9884dup
ENST00000483566.1:c.-189-25358_-189-25349dup	ENSP00000420252.1:n.-189-25358_-189-25349dup
ENST00000491190.5:c.-109-9893_-109-9884dup	ENSP00000418537.1:n.-109-9893_-109-9884dup
NM_001199642.1:c.85-25358_85-25349dup	NP_001186571.1:n.85-25358_85-25349dup
NM_183357.2:c.1135-25358_1135-25349dup	NP_899200.1:n.1135-25358_1135-25349dup
XM_005247077.2:c.1135-25358_1135-25349dup	XP_005247134.1:n.1135-25358_1135-25349dup
XM_005247078.1:c.85-25358_85-25349dup	XP_005247135.1:n.85-25358_85-25349dup
XM_006713484.1:c.-189-25358_-189-25349dup	XP_006713547.1:n.-189-25358_-189-25349dup
XM_011512358.1:c.1135-25358_1135-25349dup	XP_011510660.1:n.1135-25358_1135-25349dup
XM_011512359.1:c.136-25358_136-25349dup	XP_011510661.1:n.136-25358_136-25349dup
XM_011512361.1:c.-189-25358_-189-25349dup	XP_011510663.1:n.-189-25358_-189-25349dup
XM_005247077.4:c.1135-25358_1135-25349dup	XP_005247134.1:n.1135-25358_1135-25349dup
XM_011512359.2:c.136-25358_136-25349dup	XP_011510661.1:n.136-25358_136-25349dup
XM_017005638.1:c.36+12402_36+12411dup	XP_016861127.1:n.36+12402_36+12411dup
XM_017005639.1:c.36+12856_36+12865dup	XP_016861128.1:n.36+12856_36+12865dup
NM_001378259.1:c.1135-25358_1135-25349dup	NP_001365188.1:n.1135-25358_1135-25349dup
NM_183357.3:c.1135-25358_1135-25349dup MANE Select	NP_899200.1:n.1135-25358_1135-25349dup