Canonical Allele Identifier: CA2667290384

Gene: ADCY5

Linked Data

• gnomAD v4: 3-123291383-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291388del , CM000665.2:g.123291388del	GRCh38
NC_000003.11:g.123010235del , CM000665.1:g.123010235del	GRCh37
NC_000003.10:g.124492925del	NCBI36
NG_033882.1:g.162162del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1741-8del	ENSP00000420082.2:n.1741-8del
ENST00000470367.2:c.2029-8del	ENSP00000514541.1:n.2029-8del
ENST00000483566.2:c.1741-8del	ENSP00000420252.2:n.1741-8del
ENST00000699714.1:c.1741-8del	ENSP00000514539.1:n.1741-8del
ENST00000699715.1:c.1741-8del	ENSP00000514540.1:n.1741-8del
ENST00000699716.1:c.1741-8del	ENSP00000514542.1:n.1741-8del
ENST00000699717.1:n.1467-8del
ENST00000699718.1:c.3139-8del	ENSP00000514543.1:n.3139-8del
ENST00000462833.6:c.3064-8del MANE Select	ENSP00000419361.1:n.3064-8del
ENST00000309879.9:c.2014-8del	ENSP00000308685.5:n.2014-8del
ENST00000462833.5:c.3064-8del	ENSP00000419361.1:n.3064-8del
ENST00000491190.5:c.2038-8del	ENSP00000418537.1:n.2038-8del
NM_001199642.1:c.2014-8del	NP_001186571.1:n.2014-8del
NM_183357.2:c.3064-8del	NP_899200.1:n.3064-8del
XM_005247077.2:c.3139-8del	XP_005247134.1:n.3139-8del
XM_005247078.1:c.2089-8del	XP_005247135.1:n.2089-8del
XM_006713483.1:c.2038-8del	XP_006713546.1:n.2038-8del
XM_006713484.1:c.1816-8del	XP_006713547.1:n.1816-8del
XM_011512359.1:c.2140-8del	XP_011510661.1:n.2140-8del
XM_011512360.1:c.2050-8del	XP_011510662.1:n.2050-8del
XM_011512361.1:c.1816-8del	XP_011510663.1:n.1816-8del
XM_005247077.4:c.3139-8del	XP_005247134.1:n.3139-8del
XM_011512359.2:c.2140-8del	XP_011510661.1:n.2140-8del
XM_011512360.3:c.2050-8del	XP_011510662.1:n.2050-8del
XM_017005638.1:c.2041-8del	XP_016861127.1:n.2041-8del
XM_017005639.1:c.2041-8del	XP_016861128.1:n.2041-8del
NM_001378259.1:c.3139-8del	NP_001365188.1:n.3139-8del
NM_183357.3:c.3064-8del MANE Select	NP_899200.1:n.3064-8del