Canonical Allele Identifier: CA1239072286
Gene: ADCY3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823282G= , CM000664.2:g.24823282G= GRCh38
NC_000002.11:g.25046151G= , CM000664.1:g.25046151G= GRCh37
NC_000002.10:g.24899655G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2813C= ENSP00000384484.2:p.Thr938=
ENST00000679454.1:c.2810C= MANE Select ENSP00000505261.1:p.Thr937=
ENST00000260600.9:c.2810C= ENSP00000260600.5:p.Thr937=
ENST00000405392.5:c.2813C= ENSP00000384484.2:p.Thr938=
ENST00000485887.1:n.82C=
ENST00000606682.5:c.1751C= ENSP00000475652.1:p.Thr584=
NM_004036.3:c.2810C= NP_004027.2:p.Thr937=
XM_005264104.1:c.2813C= XP_005264161.1:p.Thr938=
XM_005264105.1:c.2810C= XP_005264162.1:p.Thr937=
XM_006711925.1:c.2879C= XP_006711988.1:p.Thr960=
XM_011532489.1:c.2936C= XP_011530791.1:p.Thr979=
XM_011532490.1:c.2933C= XP_011530792.1:p.Thr978=
XM_011532491.1:c.2870C= XP_011530793.1:p.Thr957=
XM_011532492.1:c.2936C= XP_011530794.1:p.Thr979=
XM_011532493.1:c.2798C= XP_011530795.1:p.Thr933=
XM_011532494.1:c.2738C= XP_011530796.1:p.Thr913=
XM_011532495.1:c.2270C= XP_011530797.1:p.Thr757=
XM_011532496.1:c.2213C= XP_011530798.1:p.Thr738=
NM_001320613.1:c.2813C= NP_001307542.1:p.Thr938=
NM_004036.4:c.2810C= NP_004027.2:p.Thr937=
XM_011532492.2:c.2936C= XP_011530794.1:p.Thr979=
XM_017003186.1:c.2876C= XP_016858675.1:p.Thr959=
XM_017003187.1:c.2867C= XP_016858676.1:p.Thr956=
XM_017003188.1:c.2933C= XP_016858677.1:p.Thr978=
XM_017003189.1:c.2795C= XP_016858678.1:p.Thr932=
XM_017003190.1:c.2672C= XP_016858679.1:p.Thr891=
XM_017003191.1:c.2300C= XP_016858680.1:p.Thr767=
XM_017003192.1:c.2090C= XP_016858681.1:p.Thr697=
XM_017003193.1:c.2087C= XP_016858682.1:p.Thr696=
NM_001320613.2:c.2813C= NP_001307542.1:p.Thr938=
NM_001377128.1:c.2876C= NP_001364057.1:p.Thr959=
NM_001377129.1:c.2672C= NP_001364058.1:p.Thr891=
NM_001377130.1:c.2332-652C= NP_001364059.1:n.2332-652C=
NM_001377131.1:c.2087C= NP_001364060.1:p.Thr696=
NM_001377132.1:c.2810C= NP_001364061.1:p.Thr937=
NM_004036.5:c.2810C= MANE Select NP_004027.2:p.Thr937=