Canonical Allele Identifier: CA346062939

Gene: ADCY3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2782G>T	ENSP00000384484.2:p.Ala928Ser
ENST00000679454.1:c.2779G>T MANE Select	ENSP00000505261.1:p.Ala927Ser
ENST00000260600.9:c.2779G>T	ENSP00000260600.5:p.Ala927Ser
ENST00000405392.5:c.2782G>T	ENSP00000384484.2:p.Ala928Ser
ENST00000485887.1:n.51G>T
ENST00000606682.5:c.1720G>T	ENSP00000475652.1:p.Ala574Ser
NM_004036.3:c.2779G>T	NP_004027.2:p.Ala927Ser
XM_005264104.1:c.2782G>T	XP_005264161.1:p.Ala928Ser
XM_005264105.1:c.2779G>T	XP_005264162.1:p.Ala927Ser
XM_006711925.1:c.2848G>T	XP_006711988.1:p.Ala950Ser
XM_011532489.1:c.2905G>T	XP_011530791.1:p.Ala969Ser
XM_011532490.1:c.2902G>T	XP_011530792.1:p.Ala968Ser
XM_011532491.1:c.2839G>T	XP_011530793.1:p.Ala947Ser
XM_011532492.1:c.2905G>T	XP_011530794.1:p.Ala969Ser
XM_011532493.1:c.2767G>T	XP_011530795.1:p.Ala923Ser
XM_011532494.1:c.2707G>T	XP_011530796.1:p.Ala903Ser
XM_011532495.1:c.2239G>T	XP_011530797.1:p.Ala747Ser
XM_011532496.1:c.2182G>T	XP_011530798.1:p.Ala728Ser
NM_001320613.1:c.2782G>T	NP_001307542.1:p.Ala928Ser
NM_004036.4:c.2779G>T	NP_004027.2:p.Ala927Ser
XM_011532492.2:c.2905G>T	XP_011530794.1:p.Ala969Ser
XM_017003186.1:c.2845G>T	XP_016858675.1:p.Ala949Ser
XM_017003187.1:c.2836G>T	XP_016858676.1:p.Ala946Ser
XM_017003188.1:c.2902G>T	XP_016858677.1:p.Ala968Ser
XM_017003189.1:c.2764G>T	XP_016858678.1:p.Ala922Ser
XM_017003190.1:c.2641G>T	XP_016858679.1:p.Ala881Ser
XM_017003191.1:c.2269G>T	XP_016858680.1:p.Ala757Ser
XM_017003192.1:c.2059G>T	XP_016858681.1:p.Ala687Ser
XM_017003193.1:c.2056G>T	XP_016858682.1:p.Ala686Ser
NM_001320613.2:c.2782G>T	NP_001307542.1:p.Ala928Ser
NM_001377128.1:c.2845G>T	NP_001364057.1:p.Ala949Ser
NM_001377129.1:c.2641G>T	NP_001364058.1:p.Ala881Ser
NM_001377130.1:c.2332-683G>T	NP_001364059.1:n.2332-683G>T
NM_001377131.1:c.2056G>T	NP_001364060.1:p.Ala686Ser
NM_001377132.1:c.2779G>T	NP_001364061.1:p.Ala927Ser
NM_004036.5:c.2779G>T MANE Select	NP_004027.2:p.Ala927Ser