Canonical Allele Identifier: CA1239072278
Gene: ADCY3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823255A= , CM000664.2:g.24823255A= GRCh38
NC_000002.11:g.25046124A= , CM000664.1:g.25046124A= GRCh37
NC_000002.10:g.24899628A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2840T= ENSP00000384484.2:p.Ile947=
ENST00000679454.1:c.2837T= MANE Select ENSP00000505261.1:p.Ile946=
ENST00000260600.9:c.2837T= ENSP00000260600.5:p.Ile946=
ENST00000405392.5:c.2840T= ENSP00000384484.2:p.Ile947=
ENST00000485887.1:n.109T=
ENST00000606682.5:c.1778T= ENSP00000475652.1:p.Ile593=
NM_004036.3:c.2837T= NP_004027.2:p.Ile946=
XM_005264104.1:c.2840T= XP_005264161.1:p.Ile947=
XM_005264105.1:c.2837T= XP_005264162.1:p.Ile946=
XM_006711925.1:c.2906T= XP_006711988.1:p.Ile969=
XM_011532489.1:c.2963T= XP_011530791.1:p.Ile988=
XM_011532490.1:c.2960T= XP_011530792.1:p.Ile987=
XM_011532491.1:c.2897T= XP_011530793.1:p.Ile966=
XM_011532492.1:c.2963T= XP_011530794.1:p.Ile988=
XM_011532493.1:c.2825T= XP_011530795.1:p.Ile942=
XM_011532494.1:c.2765T= XP_011530796.1:p.Ile922=
XM_011532495.1:c.2297T= XP_011530797.1:p.Ile766=
XM_011532496.1:c.2240T= XP_011530798.1:p.Ile747=
NM_001320613.1:c.2840T= NP_001307542.1:p.Ile947=
NM_004036.4:c.2837T= NP_004027.2:p.Ile946=
XM_011532492.2:c.2963T= XP_011530794.1:p.Ile988=
XM_017003186.1:c.2903T= XP_016858675.1:p.Ile968=
XM_017003187.1:c.2894T= XP_016858676.1:p.Ile965=
XM_017003188.1:c.2960T= XP_016858677.1:p.Ile987=
XM_017003189.1:c.2822T= XP_016858678.1:p.Ile941=
XM_017003190.1:c.2699T= XP_016858679.1:p.Ile900=
XM_017003191.1:c.2327T= XP_016858680.1:p.Ile776=
XM_017003192.1:c.2117T= XP_016858681.1:p.Ile706=
XM_017003193.1:c.2114T= XP_016858682.1:p.Ile705=
NM_001320613.2:c.2840T= NP_001307542.1:p.Ile947=
NM_001377128.1:c.2903T= NP_001364057.1:p.Ile968=
NM_001377129.1:c.2699T= NP_001364058.1:p.Ile900=
NM_001377130.1:c.2332-625T= NP_001364059.1:n.2332-625T=
NM_001377131.1:c.2114T= NP_001364060.1:p.Ile705=
NM_001377132.1:c.2837T= NP_001364061.1:p.Ile946=
NM_004036.5:c.2837T= MANE Select NP_004027.2:p.Ile946=