Canonical Allele Identifier: CA346062784
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823280C>A , CM000664.2:g.24823280C>A GRCh38
NC_000002.11:g.25046149C>A , CM000664.1:g.25046149C>A GRCh37
NC_000002.10:g.24899653C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2815G>T ENSP00000384484.2:p.Glu939Ter
ENST00000679454.1:c.2812G>T MANE Select ENSP00000505261.1:p.Glu938Ter
ENST00000260600.9:c.2812G>T ENSP00000260600.5:p.Glu938Ter
ENST00000405392.5:c.2815G>T ENSP00000384484.2:p.Glu939Ter
ENST00000485887.1:n.84G>T
ENST00000606682.5:c.1753G>T ENSP00000475652.1:p.Glu585Ter
NM_004036.3:c.2812G>T NP_004027.2:p.Glu938Ter
XM_005264104.1:c.2815G>T XP_005264161.1:p.Glu939Ter
XM_005264105.1:c.2812G>T XP_005264162.1:p.Glu938Ter
XM_006711925.1:c.2881G>T XP_006711988.1:p.Glu961Ter
XM_011532489.1:c.2938G>T XP_011530791.1:p.Glu980Ter
XM_011532490.1:c.2935G>T XP_011530792.1:p.Glu979Ter
XM_011532491.1:c.2872G>T XP_011530793.1:p.Glu958Ter
XM_011532492.1:c.2938G>T XP_011530794.1:p.Glu980Ter
XM_011532493.1:c.2800G>T XP_011530795.1:p.Glu934Ter
XM_011532494.1:c.2740G>T XP_011530796.1:p.Glu914Ter
XM_011532495.1:c.2272G>T XP_011530797.1:p.Glu758Ter
XM_011532496.1:c.2215G>T XP_011530798.1:p.Glu739Ter
NM_001320613.1:c.2815G>T NP_001307542.1:p.Glu939Ter
NM_004036.4:c.2812G>T NP_004027.2:p.Glu938Ter
XM_011532492.2:c.2938G>T XP_011530794.1:p.Glu980Ter
XM_017003186.1:c.2878G>T XP_016858675.1:p.Glu960Ter
XM_017003187.1:c.2869G>T XP_016858676.1:p.Glu957Ter
XM_017003188.1:c.2935G>T XP_016858677.1:p.Glu979Ter
XM_017003189.1:c.2797G>T XP_016858678.1:p.Glu933Ter
XM_017003190.1:c.2674G>T XP_016858679.1:p.Glu892Ter
XM_017003191.1:c.2302G>T XP_016858680.1:p.Glu768Ter
XM_017003192.1:c.2092G>T XP_016858681.1:p.Glu698Ter
XM_017003193.1:c.2089G>T XP_016858682.1:p.Glu697Ter
NM_001320613.2:c.2815G>T NP_001307542.1:p.Glu939Ter
NM_001377128.1:c.2878G>T NP_001364057.1:p.Glu960Ter
NM_001377129.1:c.2674G>T NP_001364058.1:p.Glu892Ter
NM_001377130.1:c.2332-650G>T NP_001364059.1:n.2332-650G>T
NM_001377131.1:c.2089G>T NP_001364060.1:p.Glu697Ter
NM_001377132.1:c.2812G>T NP_001364061.1:p.Glu938Ter
NM_004036.5:c.2812G>T MANE Select NP_004027.2:p.Glu938Ter