Canonical Allele Identifier: CA346063017
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823332A>T , CM000664.2:g.24823332A>T GRCh38
NC_000002.11:g.25046201A>T , CM000664.1:g.25046201A>T GRCh37
NC_000002.10:g.24899705A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2763T>A ENSP00000384484.2:p.Asp921Glu
ENST00000679454.1:c.2760T>A MANE Select ENSP00000505261.1:p.Asp920Glu
ENST00000260600.9:c.2760T>A ENSP00000260600.5:p.Asp920Glu
ENST00000405392.5:c.2763T>A ENSP00000384484.2:p.Asp921Glu
ENST00000485887.1:n.32T>A
ENST00000606682.5:c.1701T>A ENSP00000475652.1:p.Asp567Glu
NM_004036.3:c.2760T>A NP_004027.2:p.Asp920Glu
XM_005264104.1:c.2763T>A XP_005264161.1:p.Asp921Glu
XM_005264105.1:c.2760T>A XP_005264162.1:p.Asp920Glu
XM_006711925.1:c.2829T>A XP_006711988.1:p.Asp943Glu
XM_011532489.1:c.2886T>A XP_011530791.1:p.Asp962Glu
XM_011532490.1:c.2883T>A XP_011530792.1:p.Asp961Glu
XM_011532491.1:c.2820T>A XP_011530793.1:p.Asp940Glu
XM_011532492.1:c.2886T>A XP_011530794.1:p.Asp962Glu
XM_011532493.1:c.2748T>A XP_011530795.1:p.Asp916Glu
XM_011532494.1:c.2688T>A XP_011530796.1:p.Asp896Glu
XM_011532495.1:c.2220T>A XP_011530797.1:p.Asp740Glu
XM_011532496.1:c.2163T>A XP_011530798.1:p.Asp721Glu
NM_001320613.1:c.2763T>A NP_001307542.1:p.Asp921Glu
NM_004036.4:c.2760T>A NP_004027.2:p.Asp920Glu
XM_011532492.2:c.2886T>A XP_011530794.1:p.Asp962Glu
XM_017003186.1:c.2826T>A XP_016858675.1:p.Asp942Glu
XM_017003187.1:c.2817T>A XP_016858676.1:p.Asp939Glu
XM_017003188.1:c.2883T>A XP_016858677.1:p.Asp961Glu
XM_017003189.1:c.2745T>A XP_016858678.1:p.Asp915Glu
XM_017003190.1:c.2622T>A XP_016858679.1:p.Asp874Glu
XM_017003191.1:c.2250T>A XP_016858680.1:p.Asp750Glu
XM_017003192.1:c.2040T>A XP_016858681.1:p.Asp680Glu
XM_017003193.1:c.2037T>A XP_016858682.1:p.Asp679Glu
NM_001320613.2:c.2763T>A NP_001307542.1:p.Asp921Glu
NM_001377128.1:c.2826T>A NP_001364057.1:p.Asp942Glu
NM_001377129.1:c.2622T>A NP_001364058.1:p.Asp874Glu
NM_001377130.1:c.2332-702T>A NP_001364059.1:n.2332-702T>A
NM_001377131.1:c.2037T>A NP_001364060.1:p.Asp679Glu
NM_001377132.1:c.2760T>A NP_001364061.1:p.Asp920Glu
NM_004036.5:c.2760T>A MANE Select NP_004027.2:p.Asp920Glu