Canonical Allele Identifier: CA1239072929

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824457C= , CM000664.2:g.24824457C=	GRCh38
NC_000002.11:g.25047326C= , CM000664.1:g.25047326C=	GRCh37
NC_000002.10:g.24900830C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2660G=	ENSP00000384484.2:p.Arg887=
ENST00000679454.1:c.2657G= MANE Select	ENSP00000505261.1:p.Arg886=
ENST00000260600.9:c.2657G=	ENSP00000260600.5:p.Arg886=
ENST00000405392.5:c.2660G=	ENSP00000384484.2:p.Arg887=
ENST00000606682.5:c.1598G=	ENSP00000475652.1:p.Arg533=
NM_004036.3:c.2657G=	NP_004027.2:p.Arg886=
XM_005264104.1:c.2660G=	XP_005264161.1:p.Arg887=
XM_005264105.1:c.2657G=	XP_005264162.1:p.Arg886=
XM_006711925.1:c.2726G=	XP_006711988.1:p.Arg909=
XM_011532489.1:c.2783G=	XP_011530791.1:p.Arg928=
XM_011532490.1:c.2780G=	XP_011530792.1:p.Arg927=
XM_011532491.1:c.2717G=	XP_011530793.1:p.Arg906=
XM_011532492.1:c.2783G=	XP_011530794.1:p.Arg928=
XM_011532493.1:c.2645G=	XP_011530795.1:p.Arg882=
XM_011532494.1:c.2585G=	XP_011530796.1:p.Arg862=
XM_011532495.1:c.2117G=	XP_011530797.1:p.Arg706=
XM_011532496.1:c.2060G=	XP_011530798.1:p.Arg687=
NM_001320613.1:c.2660G=	NP_001307542.1:p.Arg887=
NM_004036.4:c.2657G=	NP_004027.2:p.Arg886=
XM_011532492.2:c.2783G=	XP_011530794.1:p.Arg928=
XM_017003186.1:c.2723G=	XP_016858675.1:p.Arg908=
XM_017003187.1:c.2714G=	XP_016858676.1:p.Arg905=
XM_017003188.1:c.2780G=	XP_016858677.1:p.Arg927=
XM_017003189.1:c.2642G=	XP_016858678.1:p.Arg881=
XM_017003190.1:c.2519G=	XP_016858679.1:p.Arg840=
XM_017003191.1:c.2147G=	XP_016858680.1:p.Arg716=
XM_017003192.1:c.1937G=	XP_016858681.1:p.Arg646=
XM_017003193.1:c.1934G=	XP_016858682.1:p.Arg645=
NM_001320613.2:c.2660G=	NP_001307542.1:p.Arg887=
NM_001377128.1:c.2723G=	NP_001364057.1:p.Arg908=
NM_001377129.1:c.2519G=	NP_001364058.1:p.Arg840=
NM_001377130.1:c.2252G=	NP_001364059.1:p.Arg751=
NM_001377131.1:c.1934G=	NP_001364060.1:p.Arg645=
NM_001377132.1:c.2657G=	NP_001364061.1:p.Arg886=
NM_004036.5:c.2657G= MANE Select	NP_004027.2:p.Arg886=