Canonical Allele Identifier: CA346062538
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823235T>G , CM000664.2:g.24823235T>G GRCh38
NC_000002.11:g.25046104T>G , CM000664.1:g.25046104T>G GRCh37
NC_000002.10:g.24899608T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2860A>C ENSP00000384484.2:p.Asn954His
ENST00000679454.1:c.2857A>C MANE Select ENSP00000505261.1:p.Asn953His
ENST00000260600.9:c.2857A>C ENSP00000260600.5:p.Asn953His
ENST00000405392.5:c.2860A>C ENSP00000384484.2:p.Asn954His
ENST00000485887.1:n.129A>C
ENST00000606682.5:c.1798A>C ENSP00000475652.1:p.Asn600His
NM_004036.3:c.2857A>C NP_004027.2:p.Asn953His
XM_005264104.1:c.2860A>C XP_005264161.1:p.Asn954His
XM_005264105.1:c.2857A>C XP_005264162.1:p.Asn953His
XM_006711925.1:c.2926A>C XP_006711988.1:p.Asn976His
XM_011532489.1:c.2983A>C XP_011530791.1:p.Asn995His
XM_011532490.1:c.2980A>C XP_011530792.1:p.Asn994His
XM_011532491.1:c.2917A>C XP_011530793.1:p.Asn973His
XM_011532492.1:c.2983A>C XP_011530794.1:p.Asn995His
XM_011532493.1:c.2845A>C XP_011530795.1:p.Asn949His
XM_011532494.1:c.2785A>C XP_011530796.1:p.Asn929His
XM_011532495.1:c.2317A>C XP_011530797.1:p.Asn773His
XM_011532496.1:c.2260A>C XP_011530798.1:p.Asn754His
NM_001320613.1:c.2860A>C NP_001307542.1:p.Asn954His
NM_004036.4:c.2857A>C NP_004027.2:p.Asn953His
XM_011532492.2:c.2983A>C XP_011530794.1:p.Asn995His
XM_017003186.1:c.2923A>C XP_016858675.1:p.Asn975His
XM_017003187.1:c.2914A>C XP_016858676.1:p.Asn972His
XM_017003188.1:c.2980A>C XP_016858677.1:p.Asn994His
XM_017003189.1:c.2842A>C XP_016858678.1:p.Asn948His
XM_017003190.1:c.2719A>C XP_016858679.1:p.Asn907His
XM_017003191.1:c.2347A>C XP_016858680.1:p.Asn783His
XM_017003192.1:c.2137A>C XP_016858681.1:p.Asn713His
XM_017003193.1:c.2134A>C XP_016858682.1:p.Asn712His
NM_001320613.2:c.2860A>C NP_001307542.1:p.Asn954His
NM_001377128.1:c.2923A>C NP_001364057.1:p.Asn975His
NM_001377129.1:c.2719A>C NP_001364058.1:p.Asn907His
NM_001377130.1:c.2332-605A>C NP_001364059.1:n.2332-605A>C
NM_001377131.1:c.2134A>C NP_001364060.1:p.Asn712His
NM_001377132.1:c.2857A>C NP_001364061.1:p.Asn953His
NM_004036.5:c.2857A>C MANE Select NP_004027.2:p.Asn953His