Canonical Allele Identifier: CA425171989

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046147C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823278C>T , CM000664.2:g.24823278C>T	GRCh38
NC_000002.11:g.25046147C>T , CM000664.1:g.25046147C>T	GRCh37
NC_000002.10:g.24899651C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2817G>A	ENSP00000384484.2:p.Glu939=
ENST00000679454.1:c.2814G>A MANE Select	ENSP00000505261.1:p.Glu938=
ENST00000260600.9:c.2814G>A	ENSP00000260600.5:p.Glu938=
ENST00000405392.5:c.2817G>A	ENSP00000384484.2:p.Glu939=
ENST00000485887.1:n.86G>A
ENST00000606682.5:c.1755G>A	ENSP00000475652.1:p.Glu585=
NM_004036.3:c.2814G>A	NP_004027.2:p.Glu938=
XM_005264104.1:c.2817G>A	XP_005264161.1:p.Glu939=
XM_005264105.1:c.2814G>A	XP_005264162.1:p.Glu938=
XM_006711925.1:c.2883G>A	XP_006711988.1:p.Glu961=
XM_011532489.1:c.2940G>A	XP_011530791.1:p.Glu980=
XM_011532490.1:c.2937G>A	XP_011530792.1:p.Glu979=
XM_011532491.1:c.2874G>A	XP_011530793.1:p.Glu958=
XM_011532492.1:c.2940G>A	XP_011530794.1:p.Glu980=
XM_011532493.1:c.2802G>A	XP_011530795.1:p.Glu934=
XM_011532494.1:c.2742G>A	XP_011530796.1:p.Glu914=
XM_011532495.1:c.2274G>A	XP_011530797.1:p.Glu758=
XM_011532496.1:c.2217G>A	XP_011530798.1:p.Glu739=
NM_001320613.1:c.2817G>A	NP_001307542.1:p.Glu939=
NM_004036.4:c.2814G>A	NP_004027.2:p.Glu938=
XM_011532492.2:c.2940G>A	XP_011530794.1:p.Glu980=
XM_017003186.1:c.2880G>A	XP_016858675.1:p.Glu960=
XM_017003187.1:c.2871G>A	XP_016858676.1:p.Glu957=
XM_017003188.1:c.2937G>A	XP_016858677.1:p.Glu979=
XM_017003189.1:c.2799G>A	XP_016858678.1:p.Glu933=
XM_017003190.1:c.2676G>A	XP_016858679.1:p.Glu892=
XM_017003191.1:c.2304G>A	XP_016858680.1:p.Glu768=
XM_017003192.1:c.2094G>A	XP_016858681.1:p.Glu698=
XM_017003193.1:c.2091G>A	XP_016858682.1:p.Glu697=
NM_001320613.2:c.2817G>A	NP_001307542.1:p.Glu939=
NM_001377128.1:c.2880G>A	NP_001364057.1:p.Glu960=
NM_001377129.1:c.2676G>A	NP_001364058.1:p.Glu892=
NM_001377130.1:c.2332-648G>A	NP_001364059.1:n.2332-648G>A
NM_001377131.1:c.2091G>A	NP_001364060.1:p.Glu697=
NM_001377132.1:c.2814G>A	NP_001364061.1:p.Glu938=
NM_004036.5:c.2814G>A MANE Select	NP_004027.2:p.Glu938=