Canonical Allele Identifier: CA346063028
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823335A>C , CM000664.2:g.24823335A>C GRCh38
NC_000002.11:g.25046204A>C , CM000664.1:g.25046204A>C GRCh37
NC_000002.10:g.24899708A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2760T>G ENSP00000384484.2:p.Tyr920Ter
ENST00000679454.1:c.2757T>G MANE Select ENSP00000505261.1:p.Tyr919Ter
ENST00000260600.9:c.2757T>G ENSP00000260600.5:p.Tyr919Ter
ENST00000405392.5:c.2760T>G ENSP00000384484.2:p.Tyr920Ter
ENST00000485887.1:n.29T>G
ENST00000606682.5:c.1698T>G ENSP00000475652.1:p.Tyr566Ter
NM_004036.3:c.2757T>G NP_004027.2:p.Tyr919Ter
XM_005264104.1:c.2760T>G XP_005264161.1:p.Tyr920Ter
XM_005264105.1:c.2757T>G XP_005264162.1:p.Tyr919Ter
XM_006711925.1:c.2826T>G XP_006711988.1:p.Tyr942Ter
XM_011532489.1:c.2883T>G XP_011530791.1:p.Tyr961Ter
XM_011532490.1:c.2880T>G XP_011530792.1:p.Tyr960Ter
XM_011532491.1:c.2817T>G XP_011530793.1:p.Tyr939Ter
XM_011532492.1:c.2883T>G XP_011530794.1:p.Tyr961Ter
XM_011532493.1:c.2745T>G XP_011530795.1:p.Tyr915Ter
XM_011532494.1:c.2685T>G XP_011530796.1:p.Tyr895Ter
XM_011532495.1:c.2217T>G XP_011530797.1:p.Tyr739Ter
XM_011532496.1:c.2160T>G XP_011530798.1:p.Tyr720Ter
NM_001320613.1:c.2760T>G NP_001307542.1:p.Tyr920Ter
NM_004036.4:c.2757T>G NP_004027.2:p.Tyr919Ter
XM_011532492.2:c.2883T>G XP_011530794.1:p.Tyr961Ter
XM_017003186.1:c.2823T>G XP_016858675.1:p.Tyr941Ter
XM_017003187.1:c.2814T>G XP_016858676.1:p.Tyr938Ter
XM_017003188.1:c.2880T>G XP_016858677.1:p.Tyr960Ter
XM_017003189.1:c.2742T>G XP_016858678.1:p.Tyr914Ter
XM_017003190.1:c.2619T>G XP_016858679.1:p.Tyr873Ter
XM_017003191.1:c.2247T>G XP_016858680.1:p.Tyr749Ter
XM_017003192.1:c.2037T>G XP_016858681.1:p.Tyr679Ter
XM_017003193.1:c.2034T>G XP_016858682.1:p.Tyr678Ter
NM_001320613.2:c.2760T>G NP_001307542.1:p.Tyr920Ter
NM_001377128.1:c.2823T>G NP_001364057.1:p.Tyr941Ter
NM_001377129.1:c.2619T>G NP_001364058.1:p.Tyr873Ter
NM_001377130.1:c.2332-705T>G NP_001364059.1:n.2332-705T>G
NM_001377131.1:c.2034T>G NP_001364060.1:p.Tyr678Ter
NM_001377132.1:c.2757T>G NP_001364061.1:p.Tyr919Ter
NM_004036.5:c.2757T>G MANE Select NP_004027.2:p.Tyr919Ter