Canonical Allele Identifier: CA1239072934

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824465C= , CM000664.2:g.24824465C=	GRCh38
NC_000002.11:g.25047334C= , CM000664.1:g.25047334C=	GRCh37
NC_000002.10:g.24900838C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2652G=	ENSP00000384484.2:p.Glu884=
ENST00000679454.1:c.2649G= MANE Select	ENSP00000505261.1:p.Glu883=
ENST00000260600.9:c.2649G=	ENSP00000260600.5:p.Glu883=
ENST00000405392.5:c.2652G=	ENSP00000384484.2:p.Glu884=
ENST00000606682.5:c.1590G=	ENSP00000475652.1:p.Glu530=
NM_004036.3:c.2649G=	NP_004027.2:p.Glu883=
XM_005264104.1:c.2652G=	XP_005264161.1:p.Glu884=
XM_005264105.1:c.2649G=	XP_005264162.1:p.Glu883=
XM_006711925.1:c.2718G=	XP_006711988.1:p.Glu906=
XM_011532489.1:c.2775G=	XP_011530791.1:p.Glu925=
XM_011532490.1:c.2772G=	XP_011530792.1:p.Glu924=
XM_011532491.1:c.2709G=	XP_011530793.1:p.Glu903=
XM_011532492.1:c.2775G=	XP_011530794.1:p.Glu925=
XM_011532493.1:c.2637G=	XP_011530795.1:p.Glu879=
XM_011532494.1:c.2577G=	XP_011530796.1:p.Glu859=
XM_011532495.1:c.2109G=	XP_011530797.1:p.Glu703=
XM_011532496.1:c.2052G=	XP_011530798.1:p.Glu684=
NM_001320613.1:c.2652G=	NP_001307542.1:p.Glu884=
NM_004036.4:c.2649G=	NP_004027.2:p.Glu883=
XM_011532492.2:c.2775G=	XP_011530794.1:p.Glu925=
XM_017003186.1:c.2715G=	XP_016858675.1:p.Glu905=
XM_017003187.1:c.2706G=	XP_016858676.1:p.Glu902=
XM_017003188.1:c.2772G=	XP_016858677.1:p.Glu924=
XM_017003189.1:c.2634G=	XP_016858678.1:p.Glu878=
XM_017003190.1:c.2511G=	XP_016858679.1:p.Glu837=
XM_017003191.1:c.2139G=	XP_016858680.1:p.Glu713=
XM_017003192.1:c.1929G=	XP_016858681.1:p.Glu643=
XM_017003193.1:c.1926G=	XP_016858682.1:p.Glu642=
NM_001320613.2:c.2652G=	NP_001307542.1:p.Glu884=
NM_001377128.1:c.2715G=	NP_001364057.1:p.Glu905=
NM_001377129.1:c.2511G=	NP_001364058.1:p.Glu837=
NM_001377130.1:c.2244G=	NP_001364059.1:p.Glu748=
NM_001377131.1:c.1926G=	NP_001364060.1:p.Glu642=
NM_001377132.1:c.2649G=	NP_001364061.1:p.Glu883=
NM_004036.5:c.2649G= MANE Select	NP_004027.2:p.Glu883=