Canonical Allele Identifier: CA1239072300
Gene: ADCY3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823327A= , CM000664.2:g.24823327A= GRCh38
NC_000002.11:g.25046196A= , CM000664.1:g.25046196A= GRCh37
NC_000002.10:g.24899700A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2768T= ENSP00000384484.2:p.Ile923=
ENST00000679454.1:c.2765T= MANE Select ENSP00000505261.1:p.Ile922=
ENST00000260600.9:c.2765T= ENSP00000260600.5:p.Ile922=
ENST00000405392.5:c.2768T= ENSP00000384484.2:p.Ile923=
ENST00000485887.1:n.37T=
ENST00000606682.5:c.1706T= ENSP00000475652.1:p.Ile569=
NM_004036.3:c.2765T= NP_004027.2:p.Ile922=
XM_005264104.1:c.2768T= XP_005264161.1:p.Ile923=
XM_005264105.1:c.2765T= XP_005264162.1:p.Ile922=
XM_006711925.1:c.2834T= XP_006711988.1:p.Ile945=
XM_011532489.1:c.2891T= XP_011530791.1:p.Ile964=
XM_011532490.1:c.2888T= XP_011530792.1:p.Ile963=
XM_011532491.1:c.2825T= XP_011530793.1:p.Ile942=
XM_011532492.1:c.2891T= XP_011530794.1:p.Ile964=
XM_011532493.1:c.2753T= XP_011530795.1:p.Ile918=
XM_011532494.1:c.2693T= XP_011530796.1:p.Ile898=
XM_011532495.1:c.2225T= XP_011530797.1:p.Ile742=
XM_011532496.1:c.2168T= XP_011530798.1:p.Ile723=
NM_001320613.1:c.2768T= NP_001307542.1:p.Ile923=
NM_004036.4:c.2765T= NP_004027.2:p.Ile922=
XM_011532492.2:c.2891T= XP_011530794.1:p.Ile964=
XM_017003186.1:c.2831T= XP_016858675.1:p.Ile944=
XM_017003187.1:c.2822T= XP_016858676.1:p.Ile941=
XM_017003188.1:c.2888T= XP_016858677.1:p.Ile963=
XM_017003189.1:c.2750T= XP_016858678.1:p.Ile917=
XM_017003190.1:c.2627T= XP_016858679.1:p.Ile876=
XM_017003191.1:c.2255T= XP_016858680.1:p.Ile752=
XM_017003192.1:c.2045T= XP_016858681.1:p.Ile682=
XM_017003193.1:c.2042T= XP_016858682.1:p.Ile681=
NM_001320613.2:c.2768T= NP_001307542.1:p.Ile923=
NM_001377128.1:c.2831T= NP_001364057.1:p.Ile944=
NM_001377129.1:c.2627T= NP_001364058.1:p.Ile876=
NM_001377130.1:c.2332-697T= NP_001364059.1:n.2332-697T=
NM_001377131.1:c.2042T= NP_001364060.1:p.Ile681=
NM_001377132.1:c.2765T= NP_001364061.1:p.Ile922=
NM_004036.5:c.2765T= MANE Select NP_004027.2:p.Ile922=