Canonical Allele Identifier: CA1239072282
Gene: ADCY3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823269G= , CM000664.2:g.24823269G= GRCh38
NC_000002.11:g.25046138G= , CM000664.1:g.25046138G= GRCh37
NC_000002.10:g.24899642G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2826C= ENSP00000384484.2:p.Ile942=
ENST00000679454.1:c.2823C= MANE Select ENSP00000505261.1:p.Ile941=
ENST00000260600.9:c.2823C= ENSP00000260600.5:p.Ile941=
ENST00000405392.5:c.2826C= ENSP00000384484.2:p.Ile942=
ENST00000485887.1:n.95C=
ENST00000606682.5:c.1764C= ENSP00000475652.1:p.Ile588=
NM_004036.3:c.2823C= NP_004027.2:p.Ile941=
XM_005264104.1:c.2826C= XP_005264161.1:p.Ile942=
XM_005264105.1:c.2823C= XP_005264162.1:p.Ile941=
XM_006711925.1:c.2892C= XP_006711988.1:p.Ile964=
XM_011532489.1:c.2949C= XP_011530791.1:p.Ile983=
XM_011532490.1:c.2946C= XP_011530792.1:p.Ile982=
XM_011532491.1:c.2883C= XP_011530793.1:p.Ile961=
XM_011532492.1:c.2949C= XP_011530794.1:p.Ile983=
XM_011532493.1:c.2811C= XP_011530795.1:p.Ile937=
XM_011532494.1:c.2751C= XP_011530796.1:p.Ile917=
XM_011532495.1:c.2283C= XP_011530797.1:p.Ile761=
XM_011532496.1:c.2226C= XP_011530798.1:p.Ile742=
NM_001320613.1:c.2826C= NP_001307542.1:p.Ile942=
NM_004036.4:c.2823C= NP_004027.2:p.Ile941=
XM_011532492.2:c.2949C= XP_011530794.1:p.Ile983=
XM_017003186.1:c.2889C= XP_016858675.1:p.Ile963=
XM_017003187.1:c.2880C= XP_016858676.1:p.Ile960=
XM_017003188.1:c.2946C= XP_016858677.1:p.Ile982=
XM_017003189.1:c.2808C= XP_016858678.1:p.Ile936=
XM_017003190.1:c.2685C= XP_016858679.1:p.Ile895=
XM_017003191.1:c.2313C= XP_016858680.1:p.Ile771=
XM_017003192.1:c.2103C= XP_016858681.1:p.Ile701=
XM_017003193.1:c.2100C= XP_016858682.1:p.Ile700=
NM_001320613.2:c.2826C= NP_001307542.1:p.Ile942=
NM_001377128.1:c.2889C= NP_001364057.1:p.Ile963=
NM_001377129.1:c.2685C= NP_001364058.1:p.Ile895=
NM_001377130.1:c.2332-639C= NP_001364059.1:n.2332-639C=
NM_001377131.1:c.2100C= NP_001364060.1:p.Ile700=
NM_001377132.1:c.2823C= NP_001364061.1:p.Ile941=
NM_004036.5:c.2823C= MANE Select NP_004027.2:p.Ile941=