Canonical Allele Identifier: CA2658140090
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24824546_24824547del , CM000664.2:g.24824546_24824547del GRCh38
NC_000002.11:g.25047415_25047416del , CM000664.1:g.25047415_25047416del GRCh37
NC_000002.10:g.24900919_24900920del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000405392.6:c.2581-8_2581-7del ENSP00000384484.2:n.2581-8_2581-7del
ENST00000679454.1:c.2578-8_2578-7del MANE Select ENSP00000505261.1:n.2578-8_2578-7del
ENST00000260600.9:c.2578-8_2578-7del ENSP00000260600.5:n.2578-8_2578-7del
ENST00000405392.5:c.2581-8_2581-7del ENSP00000384484.2:n.2581-8_2581-7del
ENST00000606682.5:c.1519-8_1519-7del ENSP00000475652.1:n.1519-8_1519-7del
NM_004036.3:c.2578-8_2578-7del NP_004027.2:n.2578-8_2578-7del
XM_005264104.1:c.2581-8_2581-7del XP_005264161.1:n.2581-8_2581-7del
XM_005264105.1:c.2578-8_2578-7del XP_005264162.1:n.2578-8_2578-7del
XM_006711925.1:c.2647-8_2647-7del XP_006711988.1:n.2647-8_2647-7del
XM_011532489.1:c.2704-8_2704-7del XP_011530791.1:n.2704-8_2704-7del
XM_011532490.1:c.2701-8_2701-7del XP_011530792.1:n.2701-8_2701-7del
XM_011532491.1:c.2638-8_2638-7del XP_011530793.1:n.2638-8_2638-7del
XM_011532492.1:c.2704-8_2704-7del XP_011530794.1:n.2704-8_2704-7del
XM_011532493.1:c.2566-8_2566-7del XP_011530795.1:n.2566-8_2566-7del
XM_011532494.1:c.2506-8_2506-7del XP_011530796.1:n.2506-8_2506-7del
XM_011532495.1:c.2038-8_2038-7del XP_011530797.1:n.2038-8_2038-7del
XM_011532496.1:c.1981-8_1981-7del XP_011530798.1:n.1981-8_1981-7del
NM_001320613.1:c.2581-8_2581-7del NP_001307542.1:n.2581-8_2581-7del
NM_004036.4:c.2578-8_2578-7del NP_004027.2:n.2578-8_2578-7del
XM_011532492.2:c.2704-8_2704-7del XP_011530794.1:n.2704-8_2704-7del
XM_017003186.1:c.2644-8_2644-7del XP_016858675.1:n.2644-8_2644-7del
XM_017003187.1:c.2635-8_2635-7del XP_016858676.1:n.2635-8_2635-7del
XM_017003188.1:c.2701-8_2701-7del XP_016858677.1:n.2701-8_2701-7del
XM_017003189.1:c.2563-8_2563-7del XP_016858678.1:n.2563-8_2563-7del
XM_017003190.1:c.2440-8_2440-7del XP_016858679.1:n.2440-8_2440-7del
XM_017003191.1:c.2068-8_2068-7del XP_016858680.1:n.2068-8_2068-7del
XM_017003192.1:c.1858-8_1858-7del XP_016858681.1:n.1858-8_1858-7del
XM_017003193.1:c.1855-8_1855-7del XP_016858682.1:n.1855-8_1855-7del
NM_001320613.2:c.2581-8_2581-7del NP_001307542.1:n.2581-8_2581-7del
NM_001377128.1:c.2644-8_2644-7del NP_001364057.1:n.2644-8_2644-7del
NM_001377129.1:c.2440-8_2440-7del NP_001364058.1:n.2440-8_2440-7del
NM_001377130.1:c.2173-8_2173-7del NP_001364059.1:n.2173-8_2173-7del
NM_001377131.1:c.1855-8_1855-7del NP_001364060.1:n.1855-8_1855-7del
NM_001377132.1:c.2578-8_2578-7del NP_001364061.1:n.2578-8_2578-7del
NM_004036.5:c.2578-8_2578-7del MANE Select NP_004027.2:n.2578-8_2578-7del