Canonical Allele Identifier: CA1239076723
Gene: ADCY3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24831317_24831318delinsCA , CM000664.2:g.24831317_24831318delinsCA GRCh38
NC_000002.11:g.25054186_25054187delinsCA , CM000664.1:g.25054186_25054187delinsCA GRCh37
NC_000002.10:g.24907690_24907691delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2055+344_2055+345delinsTG ENSP00000384484.2:n.2055+344_2055+345delinsTG
ENST00000679454.1:c.2055+344_2055+345delinsTG MANE Select ENSP00000505261.1:n.2055+344_2055+345delinsTG
ENST00000260600.9:c.2055+344_2055+345delinsTG ENSP00000260600.5:n.2055+344_2055+345delinsTG
ENST00000405392.5:c.2055+344_2055+345delinsTG ENSP00000384484.2:n.2055+344_2055+345delinsTG
ENST00000450524.1:n.148+344_148+345delinsTG
ENST00000455323.1:c.72+344_72+345delinsTG ENSP00000402008.1:n.72+344_72+345delinsTG
ENST00000606682.5:c.1134+344_1134+345delinsTG ENSP00000475652.1:n.1134+344_1134+345delinsTG
NM_004036.3:c.2055+344_2055+345delinsTG NP_004027.2:n.2055+344_2055+345delinsTG
XM_005264104.1:c.2055+344_2055+345delinsTG XP_005264161.1:n.2055+344_2055+345delinsTG
XM_005264105.1:c.2055+344_2055+345delinsTG XP_005264162.1:n.2055+344_2055+345delinsTG
XM_006711925.1:c.2121+344_2121+345delinsTG XP_006711988.1:n.2121+344_2121+345delinsTG
XM_011532489.1:c.2178+344_2178+345delinsTG XP_011530791.1:n.2178+344_2178+345delinsTG
XM_011532490.1:c.2178+344_2178+345delinsTG XP_011530792.1:n.2178+344_2178+345delinsTG
XM_011532491.1:c.2112+344_2112+345delinsTG XP_011530793.1:n.2112+344_2112+345delinsTG
XM_011532492.1:c.2178+344_2178+345delinsTG XP_011530794.1:n.2178+344_2178+345delinsTG
XM_011532493.1:c.2178+344_2178+345delinsTG XP_011530795.1:n.2178+344_2178+345delinsTG
XM_011532494.1:c.2121+344_2121+345delinsTG XP_011530796.1:n.2121+344_2121+345delinsTG
XM_011532495.1:c.1512+344_1512+345delinsTG XP_011530797.1:n.1512+344_1512+345delinsTG
XM_011532496.1:c.1455+344_1455+345delinsTG XP_011530798.1:n.1455+344_1455+345delinsTG
NM_001320613.1:c.2055+344_2055+345delinsTG NP_001307542.1:n.2055+344_2055+345delinsTG
NM_004036.4:c.2055+344_2055+345delinsTG NP_004027.2:n.2055+344_2055+345delinsTG
XM_011532492.2:c.2178+344_2178+345delinsTG XP_011530794.1:n.2178+344_2178+345delinsTG
XM_017003186.1:c.2121+344_2121+345delinsTG XP_016858675.1:n.2121+344_2121+345delinsTG
XM_017003187.1:c.2112+344_2112+345delinsTG XP_016858676.1:n.2112+344_2112+345delinsTG
XM_017003188.1:c.2178+344_2178+345delinsTG XP_016858677.1:n.2178+344_2178+345delinsTG
XM_017003189.1:c.2178+344_2178+345delinsTG XP_016858678.1:n.2178+344_2178+345delinsTG
XM_017003190.1:c.2055+344_2055+345delinsTG XP_016858679.1:n.2055+344_2055+345delinsTG
XM_017003191.1:c.1542+344_1542+345delinsTG XP_016858680.1:n.1542+344_1542+345delinsTG
XM_017003192.1:c.1332+344_1332+345delinsTG XP_016858681.1:n.1332+344_1332+345delinsTG
XM_017003193.1:c.1332+344_1332+345delinsTG XP_016858682.1:n.1332+344_1332+345delinsTG
NM_001320613.2:c.2055+344_2055+345delinsTG NP_001307542.1:n.2055+344_2055+345delinsTG
NM_001377128.1:c.2121+344_2121+345delinsTG NP_001364057.1:n.2121+344_2121+345delinsTG
NM_001377129.1:c.2055+344_2055+345delinsTG NP_001364058.1:n.2055+344_2055+345delinsTG
NM_001377130.1:c.2055+344_2055+345delinsTG NP_001364059.1:n.2055+344_2055+345delinsTG
NM_001377131.1:c.1332+344_1332+345delinsTG NP_001364060.1:n.1332+344_1332+345delinsTG
NM_001377132.1:c.2055+344_2055+345delinsTG NP_001364061.1:n.2055+344_2055+345delinsTG
NM_004036.5:c.2055+344_2055+345delinsTG MANE Select NP_004027.2:n.2055+344_2055+345delinsTG