Canonical Allele Identifier: CA1239072936

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824469T= , CM000664.2:g.24824469T=	GRCh38
NC_000002.11:g.25047338T= , CM000664.1:g.25047338T=	GRCh37
NC_000002.10:g.24900842T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2648A=	ENSP00000384484.2:p.Tyr883=
ENST00000679454.1:c.2645A= MANE Select	ENSP00000505261.1:p.Tyr882=
ENST00000260600.9:c.2645A=	ENSP00000260600.5:p.Tyr882=
ENST00000405392.5:c.2648A=	ENSP00000384484.2:p.Tyr883=
ENST00000606682.5:c.1586A=	ENSP00000475652.1:p.Tyr529=
NM_004036.3:c.2645A=	NP_004027.2:p.Tyr882=
XM_005264104.1:c.2648A=	XP_005264161.1:p.Tyr883=
XM_005264105.1:c.2645A=	XP_005264162.1:p.Tyr882=
XM_006711925.1:c.2714A=	XP_006711988.1:p.Tyr905=
XM_011532489.1:c.2771A=	XP_011530791.1:p.Tyr924=
XM_011532490.1:c.2768A=	XP_011530792.1:p.Tyr923=
XM_011532491.1:c.2705A=	XP_011530793.1:p.Tyr902=
XM_011532492.1:c.2771A=	XP_011530794.1:p.Tyr924=
XM_011532493.1:c.2633A=	XP_011530795.1:p.Tyr878=
XM_011532494.1:c.2573A=	XP_011530796.1:p.Tyr858=
XM_011532495.1:c.2105A=	XP_011530797.1:p.Tyr702=
XM_011532496.1:c.2048A=	XP_011530798.1:p.Tyr683=
NM_001320613.1:c.2648A=	NP_001307542.1:p.Tyr883=
NM_004036.4:c.2645A=	NP_004027.2:p.Tyr882=
XM_011532492.2:c.2771A=	XP_011530794.1:p.Tyr924=
XM_017003186.1:c.2711A=	XP_016858675.1:p.Tyr904=
XM_017003187.1:c.2702A=	XP_016858676.1:p.Tyr901=
XM_017003188.1:c.2768A=	XP_016858677.1:p.Tyr923=
XM_017003189.1:c.2630A=	XP_016858678.1:p.Tyr877=
XM_017003190.1:c.2507A=	XP_016858679.1:p.Tyr836=
XM_017003191.1:c.2135A=	XP_016858680.1:p.Tyr712=
XM_017003192.1:c.1925A=	XP_016858681.1:p.Tyr642=
XM_017003193.1:c.1922A=	XP_016858682.1:p.Tyr641=
NM_001320613.2:c.2648A=	NP_001307542.1:p.Tyr883=
NM_001377128.1:c.2711A=	NP_001364057.1:p.Tyr904=
NM_001377129.1:c.2507A=	NP_001364058.1:p.Tyr836=
NM_001377130.1:c.2240A=	NP_001364059.1:p.Tyr747=
NM_001377131.1:c.1922A=	NP_001364060.1:p.Tyr641=
NM_001377132.1:c.2645A=	NP_001364061.1:p.Tyr882=
NM_004036.5:c.2645A= MANE Select	NP_004027.2:p.Tyr882=