Canonical Allele Identifier: CA1239072273

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823240A= , CM000664.2:g.24823240A=	GRCh38
NC_000002.11:g.25046109A= , CM000664.1:g.25046109A=	GRCh37
NC_000002.10:g.24899613A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2855T=	ENSP00000384484.2:p.Phe952=
ENST00000679454.1:c.2852T= MANE Select	ENSP00000505261.1:p.Phe951=
ENST00000260600.9:c.2852T=	ENSP00000260600.5:p.Phe951=
ENST00000405392.5:c.2855T=	ENSP00000384484.2:p.Phe952=
ENST00000485887.1:n.124T=
ENST00000606682.5:c.1793T=	ENSP00000475652.1:p.Phe598=
NM_004036.3:c.2852T=	NP_004027.2:p.Phe951=
XM_005264104.1:c.2855T=	XP_005264161.1:p.Phe952=
XM_005264105.1:c.2852T=	XP_005264162.1:p.Phe951=
XM_006711925.1:c.2921T=	XP_006711988.1:p.Phe974=
XM_011532489.1:c.2978T=	XP_011530791.1:p.Phe993=
XM_011532490.1:c.2975T=	XP_011530792.1:p.Phe992=
XM_011532491.1:c.2912T=	XP_011530793.1:p.Phe971=
XM_011532492.1:c.2978T=	XP_011530794.1:p.Phe993=
XM_011532493.1:c.2840T=	XP_011530795.1:p.Phe947=
XM_011532494.1:c.2780T=	XP_011530796.1:p.Phe927=
XM_011532495.1:c.2312T=	XP_011530797.1:p.Phe771=
XM_011532496.1:c.2255T=	XP_011530798.1:p.Phe752=
NM_001320613.1:c.2855T=	NP_001307542.1:p.Phe952=
NM_004036.4:c.2852T=	NP_004027.2:p.Phe951=
XM_011532492.2:c.2978T=	XP_011530794.1:p.Phe993=
XM_017003186.1:c.2918T=	XP_016858675.1:p.Phe973=
XM_017003187.1:c.2909T=	XP_016858676.1:p.Phe970=
XM_017003188.1:c.2975T=	XP_016858677.1:p.Phe992=
XM_017003189.1:c.2837T=	XP_016858678.1:p.Phe946=
XM_017003190.1:c.2714T=	XP_016858679.1:p.Phe905=
XM_017003191.1:c.2342T=	XP_016858680.1:p.Phe781=
XM_017003192.1:c.2132T=	XP_016858681.1:p.Phe711=
XM_017003193.1:c.2129T=	XP_016858682.1:p.Phe710=
NM_001320613.2:c.2855T=	NP_001307542.1:p.Phe952=
NM_001377128.1:c.2918T=	NP_001364057.1:p.Phe973=
NM_001377129.1:c.2714T=	NP_001364058.1:p.Phe905=
NM_001377130.1:c.2332-610T=	NP_001364059.1:n.2332-610T=
NM_001377131.1:c.2129T=	NP_001364060.1:p.Phe710=
NM_001377132.1:c.2852T=	NP_001364061.1:p.Phe951=
NM_004036.5:c.2852T= MANE Select	NP_004027.2:p.Phe951=