Canonical Allele Identifier: CA2667291216

Gene: ADCY5

Linked Data

• gnomAD v4: 3-123284336-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284336A>C , CM000665.2:g.123284336A>C	GRCh38
NC_000003.11:g.123003183A>C , CM000665.1:g.123003183A>C	GRCh37
NC_000003.10:g.124485873A>C	NCBI36
NG_033882.1:g.169210T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.*272T>G	ENSP00000420082.2:n.*272T>G
ENST00000470367.2:c.*272T>G	ENSP00000514541.1:n.*272T>G
ENST00000483566.2:c.*272T>G	ENSP00000420252.2:n.*272T>G
ENST00000699714.1:c.*272T>G	ENSP00000514539.1:n.*272T>G
ENST00000699715.1:c.*272T>G	ENSP00000514540.1:n.*272T>G
ENST00000699716.1:c.*272T>G	ENSP00000514542.1:n.*272T>G
ENST00000699717.1:n.2461T>G
ENST00000699718.1:c.4133T>G	ENSP00000514543.1:n.4133T>G
ENST00000462833.6:c.*272T>G MANE Select	ENSP00000419361.1:n.*272T>G
ENST00000462833.5:c.*272T>G	ENSP00000419361.1:n.*272T>G
ENST00000491190.5:c.*272T>G	ENSP00000418537.1:n.*272T>G
NM_001199642.1:c.*272T>G	NP_001186571.1:n.*272T>G
NM_183357.2:c.4058T>G	NP_899200.1:n.4058T>G
XM_005247077.2:c.*272T>G	XP_005247134.1:n.*272T>G
XM_005247078.1:c.*272T>G	XP_005247135.1:n.*272T>G
XM_006713483.1:c.*272T>G	XP_006713546.1:n.*272T>G
XM_006713484.1:c.*272T>G	XP_006713547.1:n.*272T>G
XM_011512359.1:c.*272T>G	XP_011510661.1:n.*272T>G
XM_011512360.1:c.*272T>G	XP_011510662.1:n.*272T>G
XM_011512361.1:c.*272T>G	XP_011510663.1:n.*272T>G
XM_005247077.4:c.*272T>G	XP_005247134.1:n.*272T>G
XM_011512359.2:c.*272T>G	XP_011510661.1:n.*272T>G
XM_011512360.3:c.*272T>G	XP_011510662.1:n.*272T>G
XM_017005638.1:c.*272T>G	XP_016861127.1:n.*272T>G
XM_017005639.1:c.*272T>G	XP_016861128.1:n.*272T>G
NM_001378259.1:c.*272T>G	NP_001365188.1:n.*272T>G
NM_183357.3:c.*272T>G MANE Select	NP_899200.1:n.*272T>G