Canonical Allele Identifier: CA346062882
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823299G>C , CM000664.2:g.24823299G>C GRCh38
NC_000002.11:g.25046168G>C , CM000664.1:g.25046168G>C GRCh37
NC_000002.10:g.24899672G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2796C>G ENSP00000384484.2:p.Asn932Lys
ENST00000679454.1:c.2793C>G MANE Select ENSP00000505261.1:p.Asn931Lys
ENST00000260600.9:c.2793C>G ENSP00000260600.5:p.Asn931Lys
ENST00000405392.5:c.2796C>G ENSP00000384484.2:p.Asn932Lys
ENST00000485887.1:n.65C>G
ENST00000606682.5:c.1734C>G ENSP00000475652.1:p.Asn578Lys
NM_004036.3:c.2793C>G NP_004027.2:p.Asn931Lys
XM_005264104.1:c.2796C>G XP_005264161.1:p.Asn932Lys
XM_005264105.1:c.2793C>G XP_005264162.1:p.Asn931Lys
XM_006711925.1:c.2862C>G XP_006711988.1:p.Asn954Lys
XM_011532489.1:c.2919C>G XP_011530791.1:p.Asn973Lys
XM_011532490.1:c.2916C>G XP_011530792.1:p.Asn972Lys
XM_011532491.1:c.2853C>G XP_011530793.1:p.Asn951Lys
XM_011532492.1:c.2919C>G XP_011530794.1:p.Asn973Lys
XM_011532493.1:c.2781C>G XP_011530795.1:p.Asn927Lys
XM_011532494.1:c.2721C>G XP_011530796.1:p.Asn907Lys
XM_011532495.1:c.2253C>G XP_011530797.1:p.Asn751Lys
XM_011532496.1:c.2196C>G XP_011530798.1:p.Asn732Lys
NM_001320613.1:c.2796C>G NP_001307542.1:p.Asn932Lys
NM_004036.4:c.2793C>G NP_004027.2:p.Asn931Lys
XM_011532492.2:c.2919C>G XP_011530794.1:p.Asn973Lys
XM_017003186.1:c.2859C>G XP_016858675.1:p.Asn953Lys
XM_017003187.1:c.2850C>G XP_016858676.1:p.Asn950Lys
XM_017003188.1:c.2916C>G XP_016858677.1:p.Asn972Lys
XM_017003189.1:c.2778C>G XP_016858678.1:p.Asn926Lys
XM_017003190.1:c.2655C>G XP_016858679.1:p.Asn885Lys
XM_017003191.1:c.2283C>G XP_016858680.1:p.Asn761Lys
XM_017003192.1:c.2073C>G XP_016858681.1:p.Asn691Lys
XM_017003193.1:c.2070C>G XP_016858682.1:p.Asn690Lys
NM_001320613.2:c.2796C>G NP_001307542.1:p.Asn932Lys
NM_001377128.1:c.2859C>G NP_001364057.1:p.Asn953Lys
NM_001377129.1:c.2655C>G NP_001364058.1:p.Asn885Lys
NM_001377130.1:c.2332-669C>G NP_001364059.1:n.2332-669C>G
NM_001377131.1:c.2070C>G NP_001364060.1:p.Asn690Lys
NM_001377132.1:c.2793C>G NP_001364061.1:p.Asn931Lys
NM_004036.5:c.2793C>G MANE Select NP_004027.2:p.Asn931Lys