Canonical Allele Identifier: CA346062819

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046155A>C (hg19) ; chr2:g.24823286A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823286A>C , CM000664.2:g.24823286A>C	GRCh38
NC_000002.11:g.25046155A>C , CM000664.1:g.25046155A>C	GRCh37
NC_000002.10:g.24899659A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2809T>G	ENSP00000384484.2:p.Tyr937Asp
ENST00000679454.1:c.2806T>G MANE Select	ENSP00000505261.1:p.Tyr936Asp
ENST00000260600.9:c.2806T>G	ENSP00000260600.5:p.Tyr936Asp
ENST00000405392.5:c.2809T>G	ENSP00000384484.2:p.Tyr937Asp
ENST00000485887.1:n.78T>G
ENST00000606682.5:c.1747T>G	ENSP00000475652.1:p.Tyr583Asp
NM_004036.3:c.2806T>G	NP_004027.2:p.Tyr936Asp
XM_005264104.1:c.2809T>G	XP_005264161.1:p.Tyr937Asp
XM_005264105.1:c.2806T>G	XP_005264162.1:p.Tyr936Asp
XM_006711925.1:c.2875T>G	XP_006711988.1:p.Tyr959Asp
XM_011532489.1:c.2932T>G	XP_011530791.1:p.Tyr978Asp
XM_011532490.1:c.2929T>G	XP_011530792.1:p.Tyr977Asp
XM_011532491.1:c.2866T>G	XP_011530793.1:p.Tyr956Asp
XM_011532492.1:c.2932T>G	XP_011530794.1:p.Tyr978Asp
XM_011532493.1:c.2794T>G	XP_011530795.1:p.Tyr932Asp
XM_011532494.1:c.2734T>G	XP_011530796.1:p.Tyr912Asp
XM_011532495.1:c.2266T>G	XP_011530797.1:p.Tyr756Asp
XM_011532496.1:c.2209T>G	XP_011530798.1:p.Tyr737Asp
NM_001320613.1:c.2809T>G	NP_001307542.1:p.Tyr937Asp
NM_004036.4:c.2806T>G	NP_004027.2:p.Tyr936Asp
XM_011532492.2:c.2932T>G	XP_011530794.1:p.Tyr978Asp
XM_017003186.1:c.2872T>G	XP_016858675.1:p.Tyr958Asp
XM_017003187.1:c.2863T>G	XP_016858676.1:p.Tyr955Asp
XM_017003188.1:c.2929T>G	XP_016858677.1:p.Tyr977Asp
XM_017003189.1:c.2791T>G	XP_016858678.1:p.Tyr931Asp
XM_017003190.1:c.2668T>G	XP_016858679.1:p.Tyr890Asp
XM_017003191.1:c.2296T>G	XP_016858680.1:p.Tyr766Asp
XM_017003192.1:c.2086T>G	XP_016858681.1:p.Tyr696Asp
XM_017003193.1:c.2083T>G	XP_016858682.1:p.Tyr695Asp
NM_001320613.2:c.2809T>G	NP_001307542.1:p.Tyr937Asp
NM_001377128.1:c.2872T>G	NP_001364057.1:p.Tyr958Asp
NM_001377129.1:c.2668T>G	NP_001364058.1:p.Tyr890Asp
NM_001377130.1:c.2332-656T>G	NP_001364059.1:n.2332-656T>G
NM_001377131.1:c.2083T>G	NP_001364060.1:p.Tyr695Asp
NM_001377132.1:c.2806T>G	NP_001364061.1:p.Tyr936Asp
NM_004036.5:c.2806T>G MANE Select	NP_004027.2:p.Tyr936Asp