Canonical Allele Identifier: CA346062569
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823244G>T , CM000664.2:g.24823244G>T GRCh38
NC_000002.11:g.25046113G>T , CM000664.1:g.25046113G>T GRCh37
NC_000002.10:g.24899617G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2851C>A ENSP00000384484.2:p.Arg951Ser
ENST00000679454.1:c.2848C>A MANE Select ENSP00000505261.1:p.Arg950Ser
ENST00000260600.9:c.2848C>A ENSP00000260600.5:p.Arg950Ser
ENST00000405392.5:c.2851C>A ENSP00000384484.2:p.Arg951Ser
ENST00000485887.1:n.120C>A
ENST00000606682.5:c.1789C>A ENSP00000475652.1:p.Arg597Ser
NM_004036.3:c.2848C>A NP_004027.2:p.Arg950Ser
XM_005264104.1:c.2851C>A XP_005264161.1:p.Arg951Ser
XM_005264105.1:c.2848C>A XP_005264162.1:p.Arg950Ser
XM_006711925.1:c.2917C>A XP_006711988.1:p.Arg973Ser
XM_011532489.1:c.2974C>A XP_011530791.1:p.Arg992Ser
XM_011532490.1:c.2971C>A XP_011530792.1:p.Arg991Ser
XM_011532491.1:c.2908C>A XP_011530793.1:p.Arg970Ser
XM_011532492.1:c.2974C>A XP_011530794.1:p.Arg992Ser
XM_011532493.1:c.2836C>A XP_011530795.1:p.Arg946Ser
XM_011532494.1:c.2776C>A XP_011530796.1:p.Arg926Ser
XM_011532495.1:c.2308C>A XP_011530797.1:p.Arg770Ser
XM_011532496.1:c.2251C>A XP_011530798.1:p.Arg751Ser
NM_001320613.1:c.2851C>A NP_001307542.1:p.Arg951Ser
NM_004036.4:c.2848C>A NP_004027.2:p.Arg950Ser
XM_011532492.2:c.2974C>A XP_011530794.1:p.Arg992Ser
XM_017003186.1:c.2914C>A XP_016858675.1:p.Arg972Ser
XM_017003187.1:c.2905C>A XP_016858676.1:p.Arg969Ser
XM_017003188.1:c.2971C>A XP_016858677.1:p.Arg991Ser
XM_017003189.1:c.2833C>A XP_016858678.1:p.Arg945Ser
XM_017003190.1:c.2710C>A XP_016858679.1:p.Arg904Ser
XM_017003191.1:c.2338C>A XP_016858680.1:p.Arg780Ser
XM_017003192.1:c.2128C>A XP_016858681.1:p.Arg710Ser
XM_017003193.1:c.2125C>A XP_016858682.1:p.Arg709Ser
NM_001320613.2:c.2851C>A NP_001307542.1:p.Arg951Ser
NM_001377128.1:c.2914C>A NP_001364057.1:p.Arg972Ser
NM_001377129.1:c.2710C>A NP_001364058.1:p.Arg904Ser
NM_001377130.1:c.2332-614C>A NP_001364059.1:n.2332-614C>A
NM_001377131.1:c.2125C>A NP_001364060.1:p.Arg709Ser
NM_001377132.1:c.2848C>A NP_001364061.1:p.Arg950Ser
NM_004036.5:c.2848C>A MANE Select NP_004027.2:p.Arg950Ser