Canonical Allele Identifier: CA2749194185
Gene: ADCY3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823284_24823285del , CM000664.2:g.24823284_24823285del GRCh38
NC_000002.11:g.25046153_25046154del , CM000664.1:g.25046153_25046154del GRCh37
NC_000002.10:g.24899657_24899658del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2813_2814del ENSP00000384484.2:p.Thr938ArgfsTer10
ENST00000679454.1:c.2810_2811del MANE Select ENSP00000505261.1:p.Thr937ArgfsTer10
ENST00000260600.9:c.2810_2811del ENSP00000260600.5:p.Thr937ArgfsTer10
ENST00000405392.5:c.2813_2814del ENSP00000384484.2:p.Thr938ArgfsTer10
ENST00000485887.1:n.82_83del
ENST00000606682.5:c.1751_1752del ENSP00000475652.1:p.Thr584ArgfsTer10
NM_004036.3:c.2810_2811del NP_004027.2:p.Thr937ArgfsTer10
XM_005264104.1:c.2813_2814del XP_005264161.1:p.Thr938ArgfsTer10
XM_005264105.1:c.2810_2811del XP_005264162.1:p.Thr937ArgfsTer10
XM_006711925.1:c.2879_2880del XP_006711988.1:p.Thr960ArgfsTer10
XM_011532489.1:c.2936_2937del XP_011530791.1:p.Thr979ArgfsTer10
XM_011532490.1:c.2933_2934del XP_011530792.1:p.Thr978ArgfsTer10
XM_011532491.1:c.2870_2871del XP_011530793.1:p.Thr957ArgfsTer10
XM_011532492.1:c.2936_2937del XP_011530794.1:p.Thr979ArgfsTer10
XM_011532493.1:c.2798_2799del XP_011530795.1:p.Thr933ArgfsTer10
XM_011532494.1:c.2738_2739del XP_011530796.1:p.Thr913ArgfsTer10
XM_011532495.1:c.2270_2271del XP_011530797.1:p.Thr757ArgfsTer10
XM_011532496.1:c.2213_2214del XP_011530798.1:p.Thr738ArgfsTer10
NM_001320613.1:c.2813_2814del NP_001307542.1:p.Thr938ArgfsTer10
NM_004036.4:c.2810_2811del NP_004027.2:p.Thr937ArgfsTer10
XM_011532492.2:c.2936_2937del XP_011530794.1:p.Thr979ArgfsTer10
XM_017003186.1:c.2876_2877del XP_016858675.1:p.Thr959ArgfsTer10
XM_017003187.1:c.2867_2868del XP_016858676.1:p.Thr956ArgfsTer10
XM_017003188.1:c.2933_2934del XP_016858677.1:p.Thr978ArgfsTer10
XM_017003189.1:c.2795_2796del XP_016858678.1:p.Thr932ArgfsTer10
XM_017003190.1:c.2672_2673del XP_016858679.1:p.Thr891ArgfsTer10
XM_017003191.1:c.2300_2301del XP_016858680.1:p.Thr767ArgfsTer10
XM_017003192.1:c.2090_2091del XP_016858681.1:p.Thr697ArgfsTer10
XM_017003193.1:c.2087_2088del XP_016858682.1:p.Thr696ArgfsTer10
NM_001320613.2:c.2813_2814del NP_001307542.1:p.Thr938ArgfsTer10
NM_001377128.1:c.2876_2877del NP_001364057.1:p.Thr959ArgfsTer10
NM_001377129.1:c.2672_2673del NP_001364058.1:p.Thr891ArgfsTer10
NM_001377130.1:c.2332-652_2332-651del NP_001364059.1:n.2332-652_2332-651del
NM_001377131.1:c.2087_2088del NP_001364060.1:p.Thr696ArgfsTer10
NM_001377132.1:c.2810_2811del NP_001364061.1:p.Thr937ArgfsTer10
NM_004036.5:c.2810_2811del MANE Select NP_004027.2:p.Thr937ArgfsTer10