Canonical Allele Identifier: CA1239072289
Gene: ADCY3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823297A= , CM000664.2:g.24823297A= GRCh38
NC_000002.11:g.25046166A= , CM000664.1:g.25046166A= GRCh37
NC_000002.10:g.24899670A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2798T= ENSP00000384484.2:p.Phe933=
ENST00000679454.1:c.2795T= MANE Select ENSP00000505261.1:p.Phe932=
ENST00000260600.9:c.2795T= ENSP00000260600.5:p.Phe932=
ENST00000405392.5:c.2798T= ENSP00000384484.2:p.Phe933=
ENST00000485887.1:n.67T=
ENST00000606682.5:c.1736T= ENSP00000475652.1:p.Phe579=
NM_004036.3:c.2795T= NP_004027.2:p.Phe932=
XM_005264104.1:c.2798T= XP_005264161.1:p.Phe933=
XM_005264105.1:c.2795T= XP_005264162.1:p.Phe932=
XM_006711925.1:c.2864T= XP_006711988.1:p.Phe955=
XM_011532489.1:c.2921T= XP_011530791.1:p.Phe974=
XM_011532490.1:c.2918T= XP_011530792.1:p.Phe973=
XM_011532491.1:c.2855T= XP_011530793.1:p.Phe952=
XM_011532492.1:c.2921T= XP_011530794.1:p.Phe974=
XM_011532493.1:c.2783T= XP_011530795.1:p.Phe928=
XM_011532494.1:c.2723T= XP_011530796.1:p.Phe908=
XM_011532495.1:c.2255T= XP_011530797.1:p.Phe752=
XM_011532496.1:c.2198T= XP_011530798.1:p.Phe733=
NM_001320613.1:c.2798T= NP_001307542.1:p.Phe933=
NM_004036.4:c.2795T= NP_004027.2:p.Phe932=
XM_011532492.2:c.2921T= XP_011530794.1:p.Phe974=
XM_017003186.1:c.2861T= XP_016858675.1:p.Phe954=
XM_017003187.1:c.2852T= XP_016858676.1:p.Phe951=
XM_017003188.1:c.2918T= XP_016858677.1:p.Phe973=
XM_017003189.1:c.2780T= XP_016858678.1:p.Phe927=
XM_017003190.1:c.2657T= XP_016858679.1:p.Phe886=
XM_017003191.1:c.2285T= XP_016858680.1:p.Phe762=
XM_017003192.1:c.2075T= XP_016858681.1:p.Phe692=
XM_017003193.1:c.2072T= XP_016858682.1:p.Phe691=
NM_001320613.2:c.2798T= NP_001307542.1:p.Phe933=
NM_001377128.1:c.2861T= NP_001364057.1:p.Phe954=
NM_001377129.1:c.2657T= NP_001364058.1:p.Phe886=
NM_001377130.1:c.2332-667T= NP_001364059.1:n.2332-667T=
NM_001377131.1:c.2072T= NP_001364060.1:p.Phe691=
NM_001377132.1:c.2795T= NP_001364061.1:p.Phe932=
NM_004036.5:c.2795T= MANE Select NP_004027.2:p.Phe932=