Canonical Allele Identifier: CA346062561
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823243C>G , CM000664.2:g.24823243C>G GRCh38
NC_000002.11:g.25046112C>G , CM000664.1:g.25046112C>G GRCh37
NC_000002.10:g.24899616C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2852G>C ENSP00000384484.2:p.Arg951Pro
ENST00000679454.1:c.2849G>C MANE Select ENSP00000505261.1:p.Arg950Pro
ENST00000260600.9:c.2849G>C ENSP00000260600.5:p.Arg950Pro
ENST00000405392.5:c.2852G>C ENSP00000384484.2:p.Arg951Pro
ENST00000485887.1:n.121G>C
ENST00000606682.5:c.1790G>C ENSP00000475652.1:p.Arg597Pro
NM_004036.3:c.2849G>C NP_004027.2:p.Arg950Pro
XM_005264104.1:c.2852G>C XP_005264161.1:p.Arg951Pro
XM_005264105.1:c.2849G>C XP_005264162.1:p.Arg950Pro
XM_006711925.1:c.2918G>C XP_006711988.1:p.Arg973Pro
XM_011532489.1:c.2975G>C XP_011530791.1:p.Arg992Pro
XM_011532490.1:c.2972G>C XP_011530792.1:p.Arg991Pro
XM_011532491.1:c.2909G>C XP_011530793.1:p.Arg970Pro
XM_011532492.1:c.2975G>C XP_011530794.1:p.Arg992Pro
XM_011532493.1:c.2837G>C XP_011530795.1:p.Arg946Pro
XM_011532494.1:c.2777G>C XP_011530796.1:p.Arg926Pro
XM_011532495.1:c.2309G>C XP_011530797.1:p.Arg770Pro
XM_011532496.1:c.2252G>C XP_011530798.1:p.Arg751Pro
NM_001320613.1:c.2852G>C NP_001307542.1:p.Arg951Pro
NM_004036.4:c.2849G>C NP_004027.2:p.Arg950Pro
XM_011532492.2:c.2975G>C XP_011530794.1:p.Arg992Pro
XM_017003186.1:c.2915G>C XP_016858675.1:p.Arg972Pro
XM_017003187.1:c.2906G>C XP_016858676.1:p.Arg969Pro
XM_017003188.1:c.2972G>C XP_016858677.1:p.Arg991Pro
XM_017003189.1:c.2834G>C XP_016858678.1:p.Arg945Pro
XM_017003190.1:c.2711G>C XP_016858679.1:p.Arg904Pro
XM_017003191.1:c.2339G>C XP_016858680.1:p.Arg780Pro
XM_017003192.1:c.2129G>C XP_016858681.1:p.Arg710Pro
XM_017003193.1:c.2126G>C XP_016858682.1:p.Arg709Pro
NM_001320613.2:c.2852G>C NP_001307542.1:p.Arg951Pro
NM_001377128.1:c.2915G>C NP_001364057.1:p.Arg972Pro
NM_001377129.1:c.2711G>C NP_001364058.1:p.Arg904Pro
NM_001377130.1:c.2332-613G>C NP_001364059.1:n.2332-613G>C
NM_001377131.1:c.2126G>C NP_001364060.1:p.Arg709Pro
NM_001377132.1:c.2849G>C NP_001364061.1:p.Arg950Pro
NM_004036.5:c.2849G>C MANE Select NP_004027.2:p.Arg950Pro