Canonical Allele Identifier: CA346062824
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823286A>T , CM000664.2:g.24823286A>T GRCh38
NC_000002.11:g.25046155A>T , CM000664.1:g.25046155A>T GRCh37
NC_000002.10:g.24899659A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2809T>A ENSP00000384484.2:p.Tyr937Asn
ENST00000679454.1:c.2806T>A MANE Select ENSP00000505261.1:p.Tyr936Asn
ENST00000260600.9:c.2806T>A ENSP00000260600.5:p.Tyr936Asn
ENST00000405392.5:c.2809T>A ENSP00000384484.2:p.Tyr937Asn
ENST00000485887.1:n.78T>A
ENST00000606682.5:c.1747T>A ENSP00000475652.1:p.Tyr583Asn
NM_004036.3:c.2806T>A NP_004027.2:p.Tyr936Asn
XM_005264104.1:c.2809T>A XP_005264161.1:p.Tyr937Asn
XM_005264105.1:c.2806T>A XP_005264162.1:p.Tyr936Asn
XM_006711925.1:c.2875T>A XP_006711988.1:p.Tyr959Asn
XM_011532489.1:c.2932T>A XP_011530791.1:p.Tyr978Asn
XM_011532490.1:c.2929T>A XP_011530792.1:p.Tyr977Asn
XM_011532491.1:c.2866T>A XP_011530793.1:p.Tyr956Asn
XM_011532492.1:c.2932T>A XP_011530794.1:p.Tyr978Asn
XM_011532493.1:c.2794T>A XP_011530795.1:p.Tyr932Asn
XM_011532494.1:c.2734T>A XP_011530796.1:p.Tyr912Asn
XM_011532495.1:c.2266T>A XP_011530797.1:p.Tyr756Asn
XM_011532496.1:c.2209T>A XP_011530798.1:p.Tyr737Asn
NM_001320613.1:c.2809T>A NP_001307542.1:p.Tyr937Asn
NM_004036.4:c.2806T>A NP_004027.2:p.Tyr936Asn
XM_011532492.2:c.2932T>A XP_011530794.1:p.Tyr978Asn
XM_017003186.1:c.2872T>A XP_016858675.1:p.Tyr958Asn
XM_017003187.1:c.2863T>A XP_016858676.1:p.Tyr955Asn
XM_017003188.1:c.2929T>A XP_016858677.1:p.Tyr977Asn
XM_017003189.1:c.2791T>A XP_016858678.1:p.Tyr931Asn
XM_017003190.1:c.2668T>A XP_016858679.1:p.Tyr890Asn
XM_017003191.1:c.2296T>A XP_016858680.1:p.Tyr766Asn
XM_017003192.1:c.2086T>A XP_016858681.1:p.Tyr696Asn
XM_017003193.1:c.2083T>A XP_016858682.1:p.Tyr695Asn
NM_001320613.2:c.2809T>A NP_001307542.1:p.Tyr937Asn
NM_001377128.1:c.2872T>A NP_001364057.1:p.Tyr958Asn
NM_001377129.1:c.2668T>A NP_001364058.1:p.Tyr890Asn
NM_001377130.1:c.2332-656T>A NP_001364059.1:n.2332-656T>A
NM_001377131.1:c.2083T>A NP_001364060.1:p.Tyr695Asn
NM_001377132.1:c.2806T>A NP_001364061.1:p.Tyr936Asn
NM_004036.5:c.2806T>A MANE Select NP_004027.2:p.Tyr936Asn