Canonical Allele Identifier: CA346062627

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046125T>C (hg19) ; chr2:g.24823256T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823256T>C , CM000664.2:g.24823256T>C	GRCh38
NC_000002.11:g.25046125T>C , CM000664.1:g.25046125T>C	GRCh37
NC_000002.10:g.24899629T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2839A>G	ENSP00000384484.2:p.Ile947Val
ENST00000679454.1:c.2836A>G MANE Select	ENSP00000505261.1:p.Ile946Val
ENST00000260600.9:c.2836A>G	ENSP00000260600.5:p.Ile946Val
ENST00000405392.5:c.2839A>G	ENSP00000384484.2:p.Ile947Val
ENST00000485887.1:n.108A>G
ENST00000606682.5:c.1777A>G	ENSP00000475652.1:p.Ile593Val
NM_004036.3:c.2836A>G	NP_004027.2:p.Ile946Val
XM_005264104.1:c.2839A>G	XP_005264161.1:p.Ile947Val
XM_005264105.1:c.2836A>G	XP_005264162.1:p.Ile946Val
XM_006711925.1:c.2905A>G	XP_006711988.1:p.Ile969Val
XM_011532489.1:c.2962A>G	XP_011530791.1:p.Ile988Val
XM_011532490.1:c.2959A>G	XP_011530792.1:p.Ile987Val
XM_011532491.1:c.2896A>G	XP_011530793.1:p.Ile966Val
XM_011532492.1:c.2962A>G	XP_011530794.1:p.Ile988Val
XM_011532493.1:c.2824A>G	XP_011530795.1:p.Ile942Val
XM_011532494.1:c.2764A>G	XP_011530796.1:p.Ile922Val
XM_011532495.1:c.2296A>G	XP_011530797.1:p.Ile766Val
XM_011532496.1:c.2239A>G	XP_011530798.1:p.Ile747Val
NM_001320613.1:c.2839A>G	NP_001307542.1:p.Ile947Val
NM_004036.4:c.2836A>G	NP_004027.2:p.Ile946Val
XM_011532492.2:c.2962A>G	XP_011530794.1:p.Ile988Val
XM_017003186.1:c.2902A>G	XP_016858675.1:p.Ile968Val
XM_017003187.1:c.2893A>G	XP_016858676.1:p.Ile965Val
XM_017003188.1:c.2959A>G	XP_016858677.1:p.Ile987Val
XM_017003189.1:c.2821A>G	XP_016858678.1:p.Ile941Val
XM_017003190.1:c.2698A>G	XP_016858679.1:p.Ile900Val
XM_017003191.1:c.2326A>G	XP_016858680.1:p.Ile776Val
XM_017003192.1:c.2116A>G	XP_016858681.1:p.Ile706Val
XM_017003193.1:c.2113A>G	XP_016858682.1:p.Ile705Val
NM_001320613.2:c.2839A>G	NP_001307542.1:p.Ile947Val
NM_001377128.1:c.2902A>G	NP_001364057.1:p.Ile968Val
NM_001377129.1:c.2698A>G	NP_001364058.1:p.Ile900Val
NM_001377130.1:c.2332-626A>G	NP_001364059.1:n.2332-626A>G
NM_001377131.1:c.2113A>G	NP_001364060.1:p.Ile705Val
NM_001377132.1:c.2836A>G	NP_001364061.1:p.Ile946Val
NM_004036.5:c.2836A>G MANE Select	NP_004027.2:p.Ile946Val