Canonical Allele Identifier: CA346062841
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823291T>C , CM000664.2:g.24823291T>C GRCh38
NC_000002.11:g.25046160T>C , CM000664.1:g.25046160T>C GRCh37
NC_000002.10:g.24899664T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2804A>G ENSP00000384484.2:p.Asp935Gly
ENST00000679454.1:c.2801A>G MANE Select ENSP00000505261.1:p.Asp934Gly
ENST00000260600.9:c.2801A>G ENSP00000260600.5:p.Asp934Gly
ENST00000405392.5:c.2804A>G ENSP00000384484.2:p.Asp935Gly
ENST00000485887.1:n.73A>G
ENST00000606682.5:c.1742A>G ENSP00000475652.1:p.Asp581Gly
NM_004036.3:c.2801A>G NP_004027.2:p.Asp934Gly
XM_005264104.1:c.2804A>G XP_005264161.1:p.Asp935Gly
XM_005264105.1:c.2801A>G XP_005264162.1:p.Asp934Gly
XM_006711925.1:c.2870A>G XP_006711988.1:p.Asp957Gly
XM_011532489.1:c.2927A>G XP_011530791.1:p.Asp976Gly
XM_011532490.1:c.2924A>G XP_011530792.1:p.Asp975Gly
XM_011532491.1:c.2861A>G XP_011530793.1:p.Asp954Gly
XM_011532492.1:c.2927A>G XP_011530794.1:p.Asp976Gly
XM_011532493.1:c.2789A>G XP_011530795.1:p.Asp930Gly
XM_011532494.1:c.2729A>G XP_011530796.1:p.Asp910Gly
XM_011532495.1:c.2261A>G XP_011530797.1:p.Asp754Gly
XM_011532496.1:c.2204A>G XP_011530798.1:p.Asp735Gly
NM_001320613.1:c.2804A>G NP_001307542.1:p.Asp935Gly
NM_004036.4:c.2801A>G NP_004027.2:p.Asp934Gly
XM_011532492.2:c.2927A>G XP_011530794.1:p.Asp976Gly
XM_017003186.1:c.2867A>G XP_016858675.1:p.Asp956Gly
XM_017003187.1:c.2858A>G XP_016858676.1:p.Asp953Gly
XM_017003188.1:c.2924A>G XP_016858677.1:p.Asp975Gly
XM_017003189.1:c.2786A>G XP_016858678.1:p.Asp929Gly
XM_017003190.1:c.2663A>G XP_016858679.1:p.Asp888Gly
XM_017003191.1:c.2291A>G XP_016858680.1:p.Asp764Gly
XM_017003192.1:c.2081A>G XP_016858681.1:p.Asp694Gly
XM_017003193.1:c.2078A>G XP_016858682.1:p.Asp693Gly
NM_001320613.2:c.2804A>G NP_001307542.1:p.Asp935Gly
NM_001377128.1:c.2867A>G NP_001364057.1:p.Asp956Gly
NM_001377129.1:c.2663A>G NP_001364058.1:p.Asp888Gly
NM_001377130.1:c.2332-661A>G NP_001364059.1:n.2332-661A>G
NM_001377131.1:c.2078A>G NP_001364060.1:p.Asp693Gly
NM_001377132.1:c.2801A>G NP_001364061.1:p.Asp934Gly
NM_004036.5:c.2801A>G MANE Select NP_004027.2:p.Asp934Gly