Canonical Allele Identifier: CA1239072269

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823226T= , CM000664.2:g.24823226T=	GRCh38
NC_000002.11:g.25046095T= , CM000664.1:g.25046095T=	GRCh37
NC_000002.10:g.24899599T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2869A=	ENSP00000384484.2:p.Ile957=
ENST00000679454.1:c.2866A= MANE Select	ENSP00000505261.1:p.Ile956=
ENST00000260600.9:c.2866A=	ENSP00000260600.5:p.Ile956=
ENST00000405392.5:c.2869A=	ENSP00000384484.2:p.Ile957=
ENST00000485887.1:n.138A=
ENST00000606682.5:c.1807A=	ENSP00000475652.1:p.Ile603=
NM_004036.3:c.2866A=	NP_004027.2:p.Ile956=
XM_005264104.1:c.2869A=	XP_005264161.1:p.Ile957=
XM_005264105.1:c.2866A=	XP_005264162.1:p.Ile956=
XM_006711925.1:c.2935A=	XP_006711988.1:p.Ile979=
XM_011532489.1:c.2992A=	XP_011530791.1:p.Ile998=
XM_011532490.1:c.2989A=	XP_011530792.1:p.Ile997=
XM_011532491.1:c.2926A=	XP_011530793.1:p.Ile976=
XM_011532492.1:c.2992A=	XP_011530794.1:p.Ile998=
XM_011532493.1:c.2854A=	XP_011530795.1:p.Ile952=
XM_011532494.1:c.2794A=	XP_011530796.1:p.Ile932=
XM_011532495.1:c.2326A=	XP_011530797.1:p.Ile776=
XM_011532496.1:c.2269A=	XP_011530798.1:p.Ile757=
NM_001320613.1:c.2869A=	NP_001307542.1:p.Ile957=
NM_004036.4:c.2866A=	NP_004027.2:p.Ile956=
XM_011532492.2:c.2992A=	XP_011530794.1:p.Ile998=
XM_017003186.1:c.2932A=	XP_016858675.1:p.Ile978=
XM_017003187.1:c.2923A=	XP_016858676.1:p.Ile975=
XM_017003188.1:c.2989A=	XP_016858677.1:p.Ile997=
XM_017003189.1:c.2851A=	XP_016858678.1:p.Ile951=
XM_017003190.1:c.2728A=	XP_016858679.1:p.Ile910=
XM_017003191.1:c.2356A=	XP_016858680.1:p.Ile786=
XM_017003192.1:c.2146A=	XP_016858681.1:p.Ile716=
XM_017003193.1:c.2143A=	XP_016858682.1:p.Ile715=
NM_001320613.2:c.2869A=	NP_001307542.1:p.Ile957=
NM_001377128.1:c.2932A=	NP_001364057.1:p.Ile978=
NM_001377129.1:c.2728A=	NP_001364058.1:p.Ile910=
NM_001377130.1:c.2332-596A=	NP_001364059.1:n.2332-596A=
NM_001377131.1:c.2143A=	NP_001364060.1:p.Ile715=
NM_001377132.1:c.2866A=	NP_001364061.1:p.Ile956=
NM_004036.5:c.2866A= MANE Select	NP_004027.2:p.Ile956=