Canonical Allele Identifier: CA346062861
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823295C>G , CM000664.2:g.24823295C>G GRCh38
NC_000002.11:g.25046164C>G , CM000664.1:g.25046164C>G GRCh37
NC_000002.10:g.24899668C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2800G>C ENSP00000384484.2:p.Ala934Pro
ENST00000679454.1:c.2797G>C MANE Select ENSP00000505261.1:p.Ala933Pro
ENST00000260600.9:c.2797G>C ENSP00000260600.5:p.Ala933Pro
ENST00000405392.5:c.2800G>C ENSP00000384484.2:p.Ala934Pro
ENST00000485887.1:n.69G>C
ENST00000606682.5:c.1738G>C ENSP00000475652.1:p.Ala580Pro
NM_004036.3:c.2797G>C NP_004027.2:p.Ala933Pro
XM_005264104.1:c.2800G>C XP_005264161.1:p.Ala934Pro
XM_005264105.1:c.2797G>C XP_005264162.1:p.Ala933Pro
XM_006711925.1:c.2866G>C XP_006711988.1:p.Ala956Pro
XM_011532489.1:c.2923G>C XP_011530791.1:p.Ala975Pro
XM_011532490.1:c.2920G>C XP_011530792.1:p.Ala974Pro
XM_011532491.1:c.2857G>C XP_011530793.1:p.Ala953Pro
XM_011532492.1:c.2923G>C XP_011530794.1:p.Ala975Pro
XM_011532493.1:c.2785G>C XP_011530795.1:p.Ala929Pro
XM_011532494.1:c.2725G>C XP_011530796.1:p.Ala909Pro
XM_011532495.1:c.2257G>C XP_011530797.1:p.Ala753Pro
XM_011532496.1:c.2200G>C XP_011530798.1:p.Ala734Pro
NM_001320613.1:c.2800G>C NP_001307542.1:p.Ala934Pro
NM_004036.4:c.2797G>C NP_004027.2:p.Ala933Pro
XM_011532492.2:c.2923G>C XP_011530794.1:p.Ala975Pro
XM_017003186.1:c.2863G>C XP_016858675.1:p.Ala955Pro
XM_017003187.1:c.2854G>C XP_016858676.1:p.Ala952Pro
XM_017003188.1:c.2920G>C XP_016858677.1:p.Ala974Pro
XM_017003189.1:c.2782G>C XP_016858678.1:p.Ala928Pro
XM_017003190.1:c.2659G>C XP_016858679.1:p.Ala887Pro
XM_017003191.1:c.2287G>C XP_016858680.1:p.Ala763Pro
XM_017003192.1:c.2077G>C XP_016858681.1:p.Ala693Pro
XM_017003193.1:c.2074G>C XP_016858682.1:p.Ala692Pro
NM_001320613.2:c.2800G>C NP_001307542.1:p.Ala934Pro
NM_001377128.1:c.2863G>C NP_001364057.1:p.Ala955Pro
NM_001377129.1:c.2659G>C NP_001364058.1:p.Ala887Pro
NM_001377130.1:c.2332-665G>C NP_001364059.1:n.2332-665G>C
NM_001377131.1:c.2074G>C NP_001364060.1:p.Ala692Pro
NM_001377132.1:c.2797G>C NP_001364061.1:p.Ala933Pro
NM_004036.5:c.2797G>C MANE Select NP_004027.2:p.Ala933Pro