Canonical Allele Identifier: CA346062733
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823274T>G , CM000664.2:g.24823274T>G GRCh38
NC_000002.11:g.25046143T>G , CM000664.1:g.25046143T>G GRCh37
NC_000002.10:g.24899647T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2821A>C ENSP00000384484.2:p.Ser941Arg
ENST00000679454.1:c.2818A>C MANE Select ENSP00000505261.1:p.Ser940Arg
ENST00000260600.9:c.2818A>C ENSP00000260600.5:p.Ser940Arg
ENST00000405392.5:c.2821A>C ENSP00000384484.2:p.Ser941Arg
ENST00000485887.1:n.90A>C
ENST00000606682.5:c.1759A>C ENSP00000475652.1:p.Ser587Arg
NM_004036.3:c.2818A>C NP_004027.2:p.Ser940Arg
XM_005264104.1:c.2821A>C XP_005264161.1:p.Ser941Arg
XM_005264105.1:c.2818A>C XP_005264162.1:p.Ser940Arg
XM_006711925.1:c.2887A>C XP_006711988.1:p.Ser963Arg
XM_011532489.1:c.2944A>C XP_011530791.1:p.Ser982Arg
XM_011532490.1:c.2941A>C XP_011530792.1:p.Ser981Arg
XM_011532491.1:c.2878A>C XP_011530793.1:p.Ser960Arg
XM_011532492.1:c.2944A>C XP_011530794.1:p.Ser982Arg
XM_011532493.1:c.2806A>C XP_011530795.1:p.Ser936Arg
XM_011532494.1:c.2746A>C XP_011530796.1:p.Ser916Arg
XM_011532495.1:c.2278A>C XP_011530797.1:p.Ser760Arg
XM_011532496.1:c.2221A>C XP_011530798.1:p.Ser741Arg
NM_001320613.1:c.2821A>C NP_001307542.1:p.Ser941Arg
NM_004036.4:c.2818A>C NP_004027.2:p.Ser940Arg
XM_011532492.2:c.2944A>C XP_011530794.1:p.Ser982Arg
XM_017003186.1:c.2884A>C XP_016858675.1:p.Ser962Arg
XM_017003187.1:c.2875A>C XP_016858676.1:p.Ser959Arg
XM_017003188.1:c.2941A>C XP_016858677.1:p.Ser981Arg
XM_017003189.1:c.2803A>C XP_016858678.1:p.Ser935Arg
XM_017003190.1:c.2680A>C XP_016858679.1:p.Ser894Arg
XM_017003191.1:c.2308A>C XP_016858680.1:p.Ser770Arg
XM_017003192.1:c.2098A>C XP_016858681.1:p.Ser700Arg
XM_017003193.1:c.2095A>C XP_016858682.1:p.Ser699Arg
NM_001320613.2:c.2821A>C NP_001307542.1:p.Ser941Arg
NM_001377128.1:c.2884A>C NP_001364057.1:p.Ser962Arg
NM_001377129.1:c.2680A>C NP_001364058.1:p.Ser894Arg
NM_001377130.1:c.2332-644A>C NP_001364059.1:n.2332-644A>C
NM_001377131.1:c.2095A>C NP_001364060.1:p.Ser699Arg
NM_001377132.1:c.2818A>C NP_001364061.1:p.Ser940Arg
NM_004036.5:c.2818A>C MANE Select NP_004027.2:p.Ser940Arg