Canonical Allele Identifier: CA346062566
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000405392.6:c.2851C>G ENSP00000384484.2:p.Arg951Gly
ENST00000679454.1:c.2848C>G MANE Select ENSP00000505261.1:p.Arg950Gly
ENST00000260600.9:c.2848C>G ENSP00000260600.5:p.Arg950Gly
ENST00000405392.5:c.2851C>G ENSP00000384484.2:p.Arg951Gly
ENST00000485887.1:n.120C>G
ENST00000606682.5:c.1789C>G ENSP00000475652.1:p.Arg597Gly
NM_004036.3:c.2848C>G NP_004027.2:p.Arg950Gly
XM_005264104.1:c.2851C>G XP_005264161.1:p.Arg951Gly
XM_005264105.1:c.2848C>G XP_005264162.1:p.Arg950Gly
XM_006711925.1:c.2917C>G XP_006711988.1:p.Arg973Gly
XM_011532489.1:c.2974C>G XP_011530791.1:p.Arg992Gly
XM_011532490.1:c.2971C>G XP_011530792.1:p.Arg991Gly
XM_011532491.1:c.2908C>G XP_011530793.1:p.Arg970Gly
XM_011532492.1:c.2974C>G XP_011530794.1:p.Arg992Gly
XM_011532493.1:c.2836C>G XP_011530795.1:p.Arg946Gly
XM_011532494.1:c.2776C>G XP_011530796.1:p.Arg926Gly
XM_011532495.1:c.2308C>G XP_011530797.1:p.Arg770Gly
XM_011532496.1:c.2251C>G XP_011530798.1:p.Arg751Gly
NM_001320613.1:c.2851C>G NP_001307542.1:p.Arg951Gly
NM_004036.4:c.2848C>G NP_004027.2:p.Arg950Gly
XM_011532492.2:c.2974C>G XP_011530794.1:p.Arg992Gly
XM_017003186.1:c.2914C>G XP_016858675.1:p.Arg972Gly
XM_017003187.1:c.2905C>G XP_016858676.1:p.Arg969Gly
XM_017003188.1:c.2971C>G XP_016858677.1:p.Arg991Gly
XM_017003189.1:c.2833C>G XP_016858678.1:p.Arg945Gly
XM_017003190.1:c.2710C>G XP_016858679.1:p.Arg904Gly
XM_017003191.1:c.2338C>G XP_016858680.1:p.Arg780Gly
XM_017003192.1:c.2128C>G XP_016858681.1:p.Arg710Gly
XM_017003193.1:c.2125C>G XP_016858682.1:p.Arg709Gly
NM_001320613.2:c.2851C>G NP_001307542.1:p.Arg951Gly
NM_001377128.1:c.2914C>G NP_001364057.1:p.Arg972Gly
NM_001377129.1:c.2710C>G NP_001364058.1:p.Arg904Gly
NM_001377130.1:c.2332-614C>G NP_001364059.1:n.2332-614C>G
NM_001377131.1:c.2125C>G NP_001364060.1:p.Arg709Gly
NM_001377132.1:c.2848C>G NP_001364061.1:p.Arg950Gly
NM_004036.5:c.2848C>G MANE Select NP_004027.2:p.Arg950Gly