Canonical Allele Identifier: CA346062773

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046148T>A (hg19) ; chr2:g.24823279T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823279T>A , CM000664.2:g.24823279T>A	GRCh38
NC_000002.11:g.25046148T>A , CM000664.1:g.25046148T>A	GRCh37
NC_000002.10:g.24899652T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2816A>T	ENSP00000384484.2:p.Glu939Val
ENST00000679454.1:c.2813A>T MANE Select	ENSP00000505261.1:p.Glu938Val
ENST00000260600.9:c.2813A>T	ENSP00000260600.5:p.Glu938Val
ENST00000405392.5:c.2816A>T	ENSP00000384484.2:p.Glu939Val
ENST00000485887.1:n.85A>T
ENST00000606682.5:c.1754A>T	ENSP00000475652.1:p.Glu585Val
NM_004036.3:c.2813A>T	NP_004027.2:p.Glu938Val
XM_005264104.1:c.2816A>T	XP_005264161.1:p.Glu939Val
XM_005264105.1:c.2813A>T	XP_005264162.1:p.Glu938Val
XM_006711925.1:c.2882A>T	XP_006711988.1:p.Glu961Val
XM_011532489.1:c.2939A>T	XP_011530791.1:p.Glu980Val
XM_011532490.1:c.2936A>T	XP_011530792.1:p.Glu979Val
XM_011532491.1:c.2873A>T	XP_011530793.1:p.Glu958Val
XM_011532492.1:c.2939A>T	XP_011530794.1:p.Glu980Val
XM_011532493.1:c.2801A>T	XP_011530795.1:p.Glu934Val
XM_011532494.1:c.2741A>T	XP_011530796.1:p.Glu914Val
XM_011532495.1:c.2273A>T	XP_011530797.1:p.Glu758Val
XM_011532496.1:c.2216A>T	XP_011530798.1:p.Glu739Val
NM_001320613.1:c.2816A>T	NP_001307542.1:p.Glu939Val
NM_004036.4:c.2813A>T	NP_004027.2:p.Glu938Val
XM_011532492.2:c.2939A>T	XP_011530794.1:p.Glu980Val
XM_017003186.1:c.2879A>T	XP_016858675.1:p.Glu960Val
XM_017003187.1:c.2870A>T	XP_016858676.1:p.Glu957Val
XM_017003188.1:c.2936A>T	XP_016858677.1:p.Glu979Val
XM_017003189.1:c.2798A>T	XP_016858678.1:p.Glu933Val
XM_017003190.1:c.2675A>T	XP_016858679.1:p.Glu892Val
XM_017003191.1:c.2303A>T	XP_016858680.1:p.Glu768Val
XM_017003192.1:c.2093A>T	XP_016858681.1:p.Glu698Val
XM_017003193.1:c.2090A>T	XP_016858682.1:p.Glu697Val
NM_001320613.2:c.2816A>T	NP_001307542.1:p.Glu939Val
NM_001377128.1:c.2879A>T	NP_001364057.1:p.Glu960Val
NM_001377129.1:c.2675A>T	NP_001364058.1:p.Glu892Val
NM_001377130.1:c.2332-649A>T	NP_001364059.1:n.2332-649A>T
NM_001377131.1:c.2090A>T	NP_001364060.1:p.Glu697Val
NM_001377132.1:c.2813A>T	NP_001364061.1:p.Glu938Val
NM_004036.5:c.2813A>T MANE Select	NP_004027.2:p.Glu938Val