Canonical Allele Identifier: CA2667290375
Gene: ADCY5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123291383_123291384del , CM000665.2:g.123291383_123291384del GRCh38
NC_000003.11:g.123010230_123010231del , CM000665.1:g.123010230_123010231del GRCh37
NC_000003.10:g.124492920_124492921del NCBI36
NG_033882.1:g.162166_162167del

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.1741-4_1741-3del ENSP00000420082.2:n.1741-4_1741-3del
ENST00000470367.2:c.2029-4_2029-3del ENSP00000514541.1:n.2029-4_2029-3del
ENST00000483566.2:c.1741-4_1741-3del ENSP00000420252.2:n.1741-4_1741-3del
ENST00000699714.1:c.1741-4_1741-3del ENSP00000514539.1:n.1741-4_1741-3del
ENST00000699715.1:c.1741-4_1741-3del ENSP00000514540.1:n.1741-4_1741-3del
ENST00000699716.1:c.1741-4_1741-3del ENSP00000514542.1:n.1741-4_1741-3del
ENST00000699717.1:n.1467-4_1467-3del
ENST00000699718.1:c.3139-4_3139-3del ENSP00000514543.1:n.3139-4_3139-3del
ENST00000462833.6:c.3064-4_3064-3del MANE Select ENSP00000419361.1:n.3064-4_3064-3del
ENST00000309879.9:c.2014-4_2014-3del ENSP00000308685.5:n.2014-4_2014-3del
ENST00000462833.5:c.3064-4_3064-3del ENSP00000419361.1:n.3064-4_3064-3del
ENST00000491190.5:c.2038-4_2038-3del ENSP00000418537.1:n.2038-4_2038-3del
NM_001199642.1:c.2014-4_2014-3del NP_001186571.1:n.2014-4_2014-3del
NM_183357.2:c.3064-4_3064-3del NP_899200.1:n.3064-4_3064-3del
XM_005247077.2:c.3139-4_3139-3del XP_005247134.1:n.3139-4_3139-3del
XM_005247078.1:c.2089-4_2089-3del XP_005247135.1:n.2089-4_2089-3del
XM_006713483.1:c.2038-4_2038-3del XP_006713546.1:n.2038-4_2038-3del
XM_006713484.1:c.1816-4_1816-3del XP_006713547.1:n.1816-4_1816-3del
XM_011512359.1:c.2140-4_2140-3del XP_011510661.1:n.2140-4_2140-3del
XM_011512360.1:c.2050-4_2050-3del XP_011510662.1:n.2050-4_2050-3del
XM_011512361.1:c.1816-4_1816-3del XP_011510663.1:n.1816-4_1816-3del
XM_005247077.4:c.3139-4_3139-3del XP_005247134.1:n.3139-4_3139-3del
XM_011512359.2:c.2140-4_2140-3del XP_011510661.1:n.2140-4_2140-3del
XM_011512360.3:c.2050-4_2050-3del XP_011510662.1:n.2050-4_2050-3del
XM_017005638.1:c.2041-4_2041-3del XP_016861127.1:n.2041-4_2041-3del
XM_017005639.1:c.2041-4_2041-3del XP_016861128.1:n.2041-4_2041-3del
NM_001378259.1:c.3139-4_3139-3del NP_001365188.1:n.3139-4_3139-3del
NM_183357.3:c.3064-4_3064-3del MANE Select NP_899200.1:n.3064-4_3064-3del