Canonical Allele Identifier: CA346062811
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823285T>G , CM000664.2:g.24823285T>G GRCh38
NC_000002.11:g.25046154T>G , CM000664.1:g.25046154T>G GRCh37
NC_000002.10:g.24899658T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2810A>C ENSP00000384484.2:p.Tyr937Ser
ENST00000679454.1:c.2807A>C MANE Select ENSP00000505261.1:p.Tyr936Ser
ENST00000260600.9:c.2807A>C ENSP00000260600.5:p.Tyr936Ser
ENST00000405392.5:c.2810A>C ENSP00000384484.2:p.Tyr937Ser
ENST00000485887.1:n.79A>C
ENST00000606682.5:c.1748A>C ENSP00000475652.1:p.Tyr583Ser
NM_004036.3:c.2807A>C NP_004027.2:p.Tyr936Ser
XM_005264104.1:c.2810A>C XP_005264161.1:p.Tyr937Ser
XM_005264105.1:c.2807A>C XP_005264162.1:p.Tyr936Ser
XM_006711925.1:c.2876A>C XP_006711988.1:p.Tyr959Ser
XM_011532489.1:c.2933A>C XP_011530791.1:p.Tyr978Ser
XM_011532490.1:c.2930A>C XP_011530792.1:p.Tyr977Ser
XM_011532491.1:c.2867A>C XP_011530793.1:p.Tyr956Ser
XM_011532492.1:c.2933A>C XP_011530794.1:p.Tyr978Ser
XM_011532493.1:c.2795A>C XP_011530795.1:p.Tyr932Ser
XM_011532494.1:c.2735A>C XP_011530796.1:p.Tyr912Ser
XM_011532495.1:c.2267A>C XP_011530797.1:p.Tyr756Ser
XM_011532496.1:c.2210A>C XP_011530798.1:p.Tyr737Ser
NM_001320613.1:c.2810A>C NP_001307542.1:p.Tyr937Ser
NM_004036.4:c.2807A>C NP_004027.2:p.Tyr936Ser
XM_011532492.2:c.2933A>C XP_011530794.1:p.Tyr978Ser
XM_017003186.1:c.2873A>C XP_016858675.1:p.Tyr958Ser
XM_017003187.1:c.2864A>C XP_016858676.1:p.Tyr955Ser
XM_017003188.1:c.2930A>C XP_016858677.1:p.Tyr977Ser
XM_017003189.1:c.2792A>C XP_016858678.1:p.Tyr931Ser
XM_017003190.1:c.2669A>C XP_016858679.1:p.Tyr890Ser
XM_017003191.1:c.2297A>C XP_016858680.1:p.Tyr766Ser
XM_017003192.1:c.2087A>C XP_016858681.1:p.Tyr696Ser
XM_017003193.1:c.2084A>C XP_016858682.1:p.Tyr695Ser
NM_001320613.2:c.2810A>C NP_001307542.1:p.Tyr937Ser
NM_001377128.1:c.2873A>C NP_001364057.1:p.Tyr958Ser
NM_001377129.1:c.2669A>C NP_001364058.1:p.Tyr890Ser
NM_001377130.1:c.2332-655A>C NP_001364059.1:n.2332-655A>C
NM_001377131.1:c.2084A>C NP_001364060.1:p.Tyr695Ser
NM_001377132.1:c.2807A>C NP_001364061.1:p.Tyr936Ser
NM_004036.5:c.2807A>C MANE Select NP_004027.2:p.Tyr936Ser