Canonical Allele Identifier: CA346062941

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046182C>T (hg19) ; chr2:g.24823313C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823313C>T , CM000664.2:g.24823313C>T	GRCh38
NC_000002.11:g.25046182C>T , CM000664.1:g.25046182C>T	GRCh37
NC_000002.10:g.24899686C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2782G>A	ENSP00000384484.2:p.Ala928Thr
ENST00000679454.1:c.2779G>A MANE Select	ENSP00000505261.1:p.Ala927Thr
ENST00000260600.9:c.2779G>A	ENSP00000260600.5:p.Ala927Thr
ENST00000405392.5:c.2782G>A	ENSP00000384484.2:p.Ala928Thr
ENST00000485887.1:n.51G>A
ENST00000606682.5:c.1720G>A	ENSP00000475652.1:p.Ala574Thr
NM_004036.3:c.2779G>A	NP_004027.2:p.Ala927Thr
XM_005264104.1:c.2782G>A	XP_005264161.1:p.Ala928Thr
XM_005264105.1:c.2779G>A	XP_005264162.1:p.Ala927Thr
XM_006711925.1:c.2848G>A	XP_006711988.1:p.Ala950Thr
XM_011532489.1:c.2905G>A	XP_011530791.1:p.Ala969Thr
XM_011532490.1:c.2902G>A	XP_011530792.1:p.Ala968Thr
XM_011532491.1:c.2839G>A	XP_011530793.1:p.Ala947Thr
XM_011532492.1:c.2905G>A	XP_011530794.1:p.Ala969Thr
XM_011532493.1:c.2767G>A	XP_011530795.1:p.Ala923Thr
XM_011532494.1:c.2707G>A	XP_011530796.1:p.Ala903Thr
XM_011532495.1:c.2239G>A	XP_011530797.1:p.Ala747Thr
XM_011532496.1:c.2182G>A	XP_011530798.1:p.Ala728Thr
NM_001320613.1:c.2782G>A	NP_001307542.1:p.Ala928Thr
NM_004036.4:c.2779G>A	NP_004027.2:p.Ala927Thr
XM_011532492.2:c.2905G>A	XP_011530794.1:p.Ala969Thr
XM_017003186.1:c.2845G>A	XP_016858675.1:p.Ala949Thr
XM_017003187.1:c.2836G>A	XP_016858676.1:p.Ala946Thr
XM_017003188.1:c.2902G>A	XP_016858677.1:p.Ala968Thr
XM_017003189.1:c.2764G>A	XP_016858678.1:p.Ala922Thr
XM_017003190.1:c.2641G>A	XP_016858679.1:p.Ala881Thr
XM_017003191.1:c.2269G>A	XP_016858680.1:p.Ala757Thr
XM_017003192.1:c.2059G>A	XP_016858681.1:p.Ala687Thr
XM_017003193.1:c.2056G>A	XP_016858682.1:p.Ala686Thr
NM_001320613.2:c.2782G>A	NP_001307542.1:p.Ala928Thr
NM_001377128.1:c.2845G>A	NP_001364057.1:p.Ala949Thr
NM_001377129.1:c.2641G>A	NP_001364058.1:p.Ala881Thr
NM_001377130.1:c.2332-683G>A	NP_001364059.1:n.2332-683G>A
NM_001377131.1:c.2056G>A	NP_001364060.1:p.Ala686Thr
NM_001377132.1:c.2779G>A	NP_001364061.1:p.Ala927Thr
NM_004036.5:c.2779G>A MANE Select	NP_004027.2:p.Ala927Thr