Canonical Allele Identifier: CA1239072956

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824515G= , CM000664.2:g.24824515G=	GRCh38
NC_000002.11:g.25047384G= , CM000664.1:g.25047384G=	GRCh37
NC_000002.10:g.24900888G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2602C=	ENSP00000384484.2:p.Leu868=
ENST00000679454.1:c.2599C= MANE Select	ENSP00000505261.1:p.Leu867=
ENST00000260600.9:c.2599C=	ENSP00000260600.5:p.Leu867=
ENST00000405392.5:c.2602C=	ENSP00000384484.2:p.Leu868=
ENST00000606682.5:c.1540C=	ENSP00000475652.1:p.Leu514=
NM_004036.3:c.2599C=	NP_004027.2:p.Leu867=
XM_005264104.1:c.2602C=	XP_005264161.1:p.Leu868=
XM_005264105.1:c.2599C=	XP_005264162.1:p.Leu867=
XM_006711925.1:c.2668C=	XP_006711988.1:p.Leu890=
XM_011532489.1:c.2725C=	XP_011530791.1:p.Leu909=
XM_011532490.1:c.2722C=	XP_011530792.1:p.Leu908=
XM_011532491.1:c.2659C=	XP_011530793.1:p.Leu887=
XM_011532492.1:c.2725C=	XP_011530794.1:p.Leu909=
XM_011532493.1:c.2587C=	XP_011530795.1:p.Leu863=
XM_011532494.1:c.2527C=	XP_011530796.1:p.Leu843=
XM_011532495.1:c.2059C=	XP_011530797.1:p.Leu687=
XM_011532496.1:c.2002C=	XP_011530798.1:p.Leu668=
NM_001320613.1:c.2602C=	NP_001307542.1:p.Leu868=
NM_004036.4:c.2599C=	NP_004027.2:p.Leu867=
XM_011532492.2:c.2725C=	XP_011530794.1:p.Leu909=
XM_017003186.1:c.2665C=	XP_016858675.1:p.Leu889=
XM_017003187.1:c.2656C=	XP_016858676.1:p.Leu886=
XM_017003188.1:c.2722C=	XP_016858677.1:p.Leu908=
XM_017003189.1:c.2584C=	XP_016858678.1:p.Leu862=
XM_017003190.1:c.2461C=	XP_016858679.1:p.Leu821=
XM_017003191.1:c.2089C=	XP_016858680.1:p.Leu697=
XM_017003192.1:c.1879C=	XP_016858681.1:p.Leu627=
XM_017003193.1:c.1876C=	XP_016858682.1:p.Leu626=
NM_001320613.2:c.2602C=	NP_001307542.1:p.Leu868=
NM_001377128.1:c.2665C=	NP_001364057.1:p.Leu889=
NM_001377129.1:c.2461C=	NP_001364058.1:p.Leu821=
NM_001377130.1:c.2194C=	NP_001364059.1:p.Leu732=
NM_001377131.1:c.1876C=	NP_001364060.1:p.Leu626=
NM_001377132.1:c.2599C=	NP_001364061.1:p.Leu867=
NM_004036.5:c.2599C= MANE Select	NP_004027.2:p.Leu867=