Canonical Allele Identifier: CA1398327502
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123284753_123284755delinsGGA , CM000665.2:g.123284753_123284755delinsGGA GRCh38
NC_000003.11:g.123003600_123003602delinsGGA , CM000665.1:g.123003600_123003602delinsGGA GRCh37
NC_000003.10:g.124486290_124486292delinsGGA NCBI36
NG_033882.1:g.168791_168793delinsTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.2335-19_2335-17delinsTCC ENSP00000420082.2:n.2335-19_2335-17delinsTCC
ENST00000470367.2:c.2623-19_2623-17delinsTCC ENSP00000514541.1:n.2623-19_2623-17delinsTCC
ENST00000483566.2:c.2335-19_2335-17delinsTCC ENSP00000420252.2:n.2335-19_2335-17delinsTCC
ENST00000699714.1:c.2335-19_2335-17delinsTCC ENSP00000514539.1:n.2335-19_2335-17delinsTCC
ENST00000699715.1:c.2335-19_2335-17delinsTCC ENSP00000514540.1:n.2335-19_2335-17delinsTCC
ENST00000699716.1:c.2335-19_2335-17delinsTCC ENSP00000514542.1:n.2335-19_2335-17delinsTCC
ENST00000699717.1:n.2061-19_2061-17delinsTCC
ENST00000699718.1:c.3733-19_3733-17delinsTCC ENSP00000514543.1:n.3733-19_3733-17delinsTCC
ENST00000462833.6:c.3658-19_3658-17delinsTCC MANE Select ENSP00000419361.1:n.3658-19_3658-17delinsTCC
ENST00000309879.9:c.2608-19_2608-17delinsTCC ENSP00000308685.5:n.2608-19_2608-17delinsTCC
ENST00000462833.5:c.3658-19_3658-17delinsTCC ENSP00000419361.1:n.3658-19_3658-17delinsTCC
ENST00000478092.1:n.428-19_428-17delinsTCC
ENST00000491190.5:c.2632-19_2632-17delinsTCC ENSP00000418537.1:n.2632-19_2632-17delinsTCC
NM_001199642.1:c.2608-19_2608-17delinsTCC NP_001186571.1:n.2608-19_2608-17delinsTCC
NM_183357.2:c.3658-19_3658-17delinsTCC NP_899200.1:n.3658-19_3658-17delinsTCC
XM_005247077.2:c.3733-19_3733-17delinsTCC XP_005247134.1:n.3733-19_3733-17delinsTCC
XM_005247078.1:c.2683-19_2683-17delinsTCC XP_005247135.1:n.2683-19_2683-17delinsTCC
XM_006713483.1:c.2632-19_2632-17delinsTCC XP_006713546.1:n.2632-19_2632-17delinsTCC
XM_006713484.1:c.2410-19_2410-17delinsTCC XP_006713547.1:n.2410-19_2410-17delinsTCC
XM_011512359.1:c.2734-19_2734-17delinsTCC XP_011510661.1:n.2734-19_2734-17delinsTCC
XM_011512360.1:c.2644-19_2644-17delinsTCC XP_011510662.1:n.2644-19_2644-17delinsTCC
XM_011512361.1:c.2410-19_2410-17delinsTCC XP_011510663.1:n.2410-19_2410-17delinsTCC
XM_005247077.4:c.3733-19_3733-17delinsTCC XP_005247134.1:n.3733-19_3733-17delinsTCC
XM_011512359.2:c.2734-19_2734-17delinsTCC XP_011510661.1:n.2734-19_2734-17delinsTCC
XM_011512360.3:c.2644-19_2644-17delinsTCC XP_011510662.1:n.2644-19_2644-17delinsTCC
XM_017005638.1:c.2635-19_2635-17delinsTCC XP_016861127.1:n.2635-19_2635-17delinsTCC
XM_017005639.1:c.2635-19_2635-17delinsTCC XP_016861128.1:n.2635-19_2635-17delinsTCC
NM_001378259.1:c.3733-19_3733-17delinsTCC NP_001365188.1:n.3733-19_3733-17delinsTCC
NM_183357.3:c.3658-19_3658-17delinsTCC MANE Select NP_899200.1:n.3658-19_3658-17delinsTCC