Canonical Allele Identifier: CA346063680

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047335T>A (hg19) ; chr2:g.24824466T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824466T>A , CM000664.2:g.24824466T>A	GRCh38
NC_000002.11:g.25047335T>A , CM000664.1:g.25047335T>A	GRCh37
NC_000002.10:g.24900839T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2651A>T	ENSP00000384484.2:p.Glu884Val
ENST00000679454.1:c.2648A>T MANE Select	ENSP00000505261.1:p.Glu883Val
ENST00000260600.9:c.2648A>T	ENSP00000260600.5:p.Glu883Val
ENST00000405392.5:c.2651A>T	ENSP00000384484.2:p.Glu884Val
ENST00000606682.5:c.1589A>T	ENSP00000475652.1:p.Glu530Val
NM_004036.3:c.2648A>T	NP_004027.2:p.Glu883Val
XM_005264104.1:c.2651A>T	XP_005264161.1:p.Glu884Val
XM_005264105.1:c.2648A>T	XP_005264162.1:p.Glu883Val
XM_006711925.1:c.2717A>T	XP_006711988.1:p.Glu906Val
XM_011532489.1:c.2774A>T	XP_011530791.1:p.Glu925Val
XM_011532490.1:c.2771A>T	XP_011530792.1:p.Glu924Val
XM_011532491.1:c.2708A>T	XP_011530793.1:p.Glu903Val
XM_011532492.1:c.2774A>T	XP_011530794.1:p.Glu925Val
XM_011532493.1:c.2636A>T	XP_011530795.1:p.Glu879Val
XM_011532494.1:c.2576A>T	XP_011530796.1:p.Glu859Val
XM_011532495.1:c.2108A>T	XP_011530797.1:p.Glu703Val
XM_011532496.1:c.2051A>T	XP_011530798.1:p.Glu684Val
NM_001320613.1:c.2651A>T	NP_001307542.1:p.Glu884Val
NM_004036.4:c.2648A>T	NP_004027.2:p.Glu883Val
XM_011532492.2:c.2774A>T	XP_011530794.1:p.Glu925Val
XM_017003186.1:c.2714A>T	XP_016858675.1:p.Glu905Val
XM_017003187.1:c.2705A>T	XP_016858676.1:p.Glu902Val
XM_017003188.1:c.2771A>T	XP_016858677.1:p.Glu924Val
XM_017003189.1:c.2633A>T	XP_016858678.1:p.Glu878Val
XM_017003190.1:c.2510A>T	XP_016858679.1:p.Glu837Val
XM_017003191.1:c.2138A>T	XP_016858680.1:p.Glu713Val
XM_017003192.1:c.1928A>T	XP_016858681.1:p.Glu643Val
XM_017003193.1:c.1925A>T	XP_016858682.1:p.Glu642Val
NM_001320613.2:c.2651A>T	NP_001307542.1:p.Glu884Val
NM_001377128.1:c.2714A>T	NP_001364057.1:p.Glu905Val
NM_001377129.1:c.2510A>T	NP_001364058.1:p.Glu837Val
NM_001377130.1:c.2243A>T	NP_001364059.1:p.Glu748Val
NM_001377131.1:c.1925A>T	NP_001364060.1:p.Glu642Val
NM_001377132.1:c.2648A>T	NP_001364061.1:p.Glu883Val
NM_004036.5:c.2648A>T MANE Select	NP_004027.2:p.Glu883Val