Canonical Allele Identifier: CA346062537
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2860A>G ENSP00000384484.2:p.Asn954Asp
ENST00000679454.1:c.2857A>G MANE Select ENSP00000505261.1:p.Asn953Asp
ENST00000260600.9:c.2857A>G ENSP00000260600.5:p.Asn953Asp
ENST00000405392.5:c.2860A>G ENSP00000384484.2:p.Asn954Asp
ENST00000485887.1:n.129A>G
ENST00000606682.5:c.1798A>G ENSP00000475652.1:p.Asn600Asp
NM_004036.3:c.2857A>G NP_004027.2:p.Asn953Asp
XM_005264104.1:c.2860A>G XP_005264161.1:p.Asn954Asp
XM_005264105.1:c.2857A>G XP_005264162.1:p.Asn953Asp
XM_006711925.1:c.2926A>G XP_006711988.1:p.Asn976Asp
XM_011532489.1:c.2983A>G XP_011530791.1:p.Asn995Asp
XM_011532490.1:c.2980A>G XP_011530792.1:p.Asn994Asp
XM_011532491.1:c.2917A>G XP_011530793.1:p.Asn973Asp
XM_011532492.1:c.2983A>G XP_011530794.1:p.Asn995Asp
XM_011532493.1:c.2845A>G XP_011530795.1:p.Asn949Asp
XM_011532494.1:c.2785A>G XP_011530796.1:p.Asn929Asp
XM_011532495.1:c.2317A>G XP_011530797.1:p.Asn773Asp
XM_011532496.1:c.2260A>G XP_011530798.1:p.Asn754Asp
NM_001320613.1:c.2860A>G NP_001307542.1:p.Asn954Asp
NM_004036.4:c.2857A>G NP_004027.2:p.Asn953Asp
XM_011532492.2:c.2983A>G XP_011530794.1:p.Asn995Asp
XM_017003186.1:c.2923A>G XP_016858675.1:p.Asn975Asp
XM_017003187.1:c.2914A>G XP_016858676.1:p.Asn972Asp
XM_017003188.1:c.2980A>G XP_016858677.1:p.Asn994Asp
XM_017003189.1:c.2842A>G XP_016858678.1:p.Asn948Asp
XM_017003190.1:c.2719A>G XP_016858679.1:p.Asn907Asp
XM_017003191.1:c.2347A>G XP_016858680.1:p.Asn783Asp
XM_017003192.1:c.2137A>G XP_016858681.1:p.Asn713Asp
XM_017003193.1:c.2134A>G XP_016858682.1:p.Asn712Asp
NM_001320613.2:c.2860A>G NP_001307542.1:p.Asn954Asp
NM_001377128.1:c.2923A>G NP_001364057.1:p.Asn975Asp
NM_001377129.1:c.2719A>G NP_001364058.1:p.Asn907Asp
NM_001377130.1:c.2332-605A>G NP_001364059.1:n.2332-605A>G
NM_001377131.1:c.2134A>G NP_001364060.1:p.Asn712Asp
NM_001377132.1:c.2857A>G NP_001364061.1:p.Asn953Asp
NM_004036.5:c.2857A>G MANE Select NP_004027.2:p.Asn953Asp