Canonical Allele Identifier: CA1239072295
Gene: ADCY3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823319T= , CM000664.2:g.24823319T= GRCh38
NC_000002.11:g.25046188T= , CM000664.1:g.25046188T= GRCh37
NC_000002.10:g.24899692T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2776A= ENSP00000384484.2:p.Met926=
ENST00000679454.1:c.2773A= MANE Select ENSP00000505261.1:p.Met925=
ENST00000260600.9:c.2773A= ENSP00000260600.5:p.Met925=
ENST00000405392.5:c.2776A= ENSP00000384484.2:p.Met926=
ENST00000485887.1:n.45A=
ENST00000606682.5:c.1714A= ENSP00000475652.1:p.Met572=
NM_004036.3:c.2773A= NP_004027.2:p.Met925=
XM_005264104.1:c.2776A= XP_005264161.1:p.Met926=
XM_005264105.1:c.2773A= XP_005264162.1:p.Met925=
XM_006711925.1:c.2842A= XP_006711988.1:p.Met948=
XM_011532489.1:c.2899A= XP_011530791.1:p.Met967=
XM_011532490.1:c.2896A= XP_011530792.1:p.Met966=
XM_011532491.1:c.2833A= XP_011530793.1:p.Met945=
XM_011532492.1:c.2899A= XP_011530794.1:p.Met967=
XM_011532493.1:c.2761A= XP_011530795.1:p.Met921=
XM_011532494.1:c.2701A= XP_011530796.1:p.Met901=
XM_011532495.1:c.2233A= XP_011530797.1:p.Met745=
XM_011532496.1:c.2176A= XP_011530798.1:p.Met726=
NM_001320613.1:c.2776A= NP_001307542.1:p.Met926=
NM_004036.4:c.2773A= NP_004027.2:p.Met925=
XM_011532492.2:c.2899A= XP_011530794.1:p.Met967=
XM_017003186.1:c.2839A= XP_016858675.1:p.Met947=
XM_017003187.1:c.2830A= XP_016858676.1:p.Met944=
XM_017003188.1:c.2896A= XP_016858677.1:p.Met966=
XM_017003189.1:c.2758A= XP_016858678.1:p.Met920=
XM_017003190.1:c.2635A= XP_016858679.1:p.Met879=
XM_017003191.1:c.2263A= XP_016858680.1:p.Met755=
XM_017003192.1:c.2053A= XP_016858681.1:p.Met685=
XM_017003193.1:c.2050A= XP_016858682.1:p.Met684=
NM_001320613.2:c.2776A= NP_001307542.1:p.Met926=
NM_001377128.1:c.2839A= NP_001364057.1:p.Met947=
NM_001377129.1:c.2635A= NP_001364058.1:p.Met879=
NM_001377130.1:c.2332-689A= NP_001364059.1:n.2332-689A=
NM_001377131.1:c.2050A= NP_001364060.1:p.Met684=
NM_001377132.1:c.2773A= NP_001364061.1:p.Met925=
NM_004036.5:c.2773A= MANE Select NP_004027.2:p.Met925=