Canonical Allele Identifier: CA1239072947

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824495C= , CM000664.2:g.24824495C=	GRCh38
NC_000002.11:g.25047364C= , CM000664.1:g.25047364C=	GRCh37
NC_000002.10:g.24900868C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2622G=	ENSP00000384484.2:p.Glu874=
ENST00000679454.1:c.2619G= MANE Select	ENSP00000505261.1:p.Glu873=
ENST00000260600.9:c.2619G=	ENSP00000260600.5:p.Glu873=
ENST00000405392.5:c.2622G=	ENSP00000384484.2:p.Glu874=
ENST00000606682.5:c.1560G=	ENSP00000475652.1:p.Glu520=
NM_004036.3:c.2619G=	NP_004027.2:p.Glu873=
XM_005264104.1:c.2622G=	XP_005264161.1:p.Glu874=
XM_005264105.1:c.2619G=	XP_005264162.1:p.Glu873=
XM_006711925.1:c.2688G=	XP_006711988.1:p.Glu896=
XM_011532489.1:c.2745G=	XP_011530791.1:p.Glu915=
XM_011532490.1:c.2742G=	XP_011530792.1:p.Glu914=
XM_011532491.1:c.2679G=	XP_011530793.1:p.Glu893=
XM_011532492.1:c.2745G=	XP_011530794.1:p.Glu915=
XM_011532493.1:c.2607G=	XP_011530795.1:p.Glu869=
XM_011532494.1:c.2547G=	XP_011530796.1:p.Glu849=
XM_011532495.1:c.2079G=	XP_011530797.1:p.Glu693=
XM_011532496.1:c.2022G=	XP_011530798.1:p.Glu674=
NM_001320613.1:c.2622G=	NP_001307542.1:p.Glu874=
NM_004036.4:c.2619G=	NP_004027.2:p.Glu873=
XM_011532492.2:c.2745G=	XP_011530794.1:p.Glu915=
XM_017003186.1:c.2685G=	XP_016858675.1:p.Glu895=
XM_017003187.1:c.2676G=	XP_016858676.1:p.Glu892=
XM_017003188.1:c.2742G=	XP_016858677.1:p.Glu914=
XM_017003189.1:c.2604G=	XP_016858678.1:p.Glu868=
XM_017003190.1:c.2481G=	XP_016858679.1:p.Glu827=
XM_017003191.1:c.2109G=	XP_016858680.1:p.Glu703=
XM_017003192.1:c.1899G=	XP_016858681.1:p.Glu633=
XM_017003193.1:c.1896G=	XP_016858682.1:p.Glu632=
NM_001320613.2:c.2622G=	NP_001307542.1:p.Glu874=
NM_001377128.1:c.2685G=	NP_001364057.1:p.Glu895=
NM_001377129.1:c.2481G=	NP_001364058.1:p.Glu827=
NM_001377130.1:c.2214G=	NP_001364059.1:p.Glu738=
NM_001377131.1:c.1896G=	NP_001364060.1:p.Glu632=
NM_001377132.1:c.2619G=	NP_001364061.1:p.Glu873=
NM_004036.5:c.2619G= MANE Select	NP_004027.2:p.Glu873=