Canonical Allele Identifier: CA346062923
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823307G>T , CM000664.2:g.24823307G>T GRCh38
NC_000002.11:g.25046176G>T , CM000664.1:g.25046176G>T GRCh37
NC_000002.10:g.24899680G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2788C>A ENSP00000384484.2:p.Leu930Met
ENST00000679454.1:c.2785C>A MANE Select ENSP00000505261.1:p.Leu929Met
ENST00000260600.9:c.2785C>A ENSP00000260600.5:p.Leu929Met
ENST00000405392.5:c.2788C>A ENSP00000384484.2:p.Leu930Met
ENST00000485887.1:n.57C>A
ENST00000606682.5:c.1726C>A ENSP00000475652.1:p.Leu576Met
NM_004036.3:c.2785C>A NP_004027.2:p.Leu929Met
XM_005264104.1:c.2788C>A XP_005264161.1:p.Leu930Met
XM_005264105.1:c.2785C>A XP_005264162.1:p.Leu929Met
XM_006711925.1:c.2854C>A XP_006711988.1:p.Leu952Met
XM_011532489.1:c.2911C>A XP_011530791.1:p.Leu971Met
XM_011532490.1:c.2908C>A XP_011530792.1:p.Leu970Met
XM_011532491.1:c.2845C>A XP_011530793.1:p.Leu949Met
XM_011532492.1:c.2911C>A XP_011530794.1:p.Leu971Met
XM_011532493.1:c.2773C>A XP_011530795.1:p.Leu925Met
XM_011532494.1:c.2713C>A XP_011530796.1:p.Leu905Met
XM_011532495.1:c.2245C>A XP_011530797.1:p.Leu749Met
XM_011532496.1:c.2188C>A XP_011530798.1:p.Leu730Met
NM_001320613.1:c.2788C>A NP_001307542.1:p.Leu930Met
NM_004036.4:c.2785C>A NP_004027.2:p.Leu929Met
XM_011532492.2:c.2911C>A XP_011530794.1:p.Leu971Met
XM_017003186.1:c.2851C>A XP_016858675.1:p.Leu951Met
XM_017003187.1:c.2842C>A XP_016858676.1:p.Leu948Met
XM_017003188.1:c.2908C>A XP_016858677.1:p.Leu970Met
XM_017003189.1:c.2770C>A XP_016858678.1:p.Leu924Met
XM_017003190.1:c.2647C>A XP_016858679.1:p.Leu883Met
XM_017003191.1:c.2275C>A XP_016858680.1:p.Leu759Met
XM_017003192.1:c.2065C>A XP_016858681.1:p.Leu689Met
XM_017003193.1:c.2062C>A XP_016858682.1:p.Leu688Met
NM_001320613.2:c.2788C>A NP_001307542.1:p.Leu930Met
NM_001377128.1:c.2851C>A NP_001364057.1:p.Leu951Met
NM_001377129.1:c.2647C>A NP_001364058.1:p.Leu883Met
NM_001377130.1:c.2332-677C>A NP_001364059.1:n.2332-677C>A
NM_001377131.1:c.2062C>A NP_001364060.1:p.Leu688Met
NM_001377132.1:c.2785C>A NP_001364061.1:p.Leu929Met
NM_004036.5:c.2785C>A MANE Select NP_004027.2:p.Leu929Met