Canonical Allele Identifier: CA346062947

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046184A>T (hg19) ; chr2:g.24823315A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823315A>T , CM000664.2:g.24823315A>T	GRCh38
NC_000002.11:g.25046184A>T , CM000664.1:g.25046184A>T	GRCh37
NC_000002.10:g.24899688A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2780T>A	ENSP00000384484.2:p.Phe927Tyr
ENST00000679454.1:c.2777T>A MANE Select	ENSP00000505261.1:p.Phe926Tyr
ENST00000260600.9:c.2777T>A	ENSP00000260600.5:p.Phe926Tyr
ENST00000405392.5:c.2780T>A	ENSP00000384484.2:p.Phe927Tyr
ENST00000485887.1:n.49T>A
ENST00000606682.5:c.1718T>A	ENSP00000475652.1:p.Phe573Tyr
NM_004036.3:c.2777T>A	NP_004027.2:p.Phe926Tyr
XM_005264104.1:c.2780T>A	XP_005264161.1:p.Phe927Tyr
XM_005264105.1:c.2777T>A	XP_005264162.1:p.Phe926Tyr
XM_006711925.1:c.2846T>A	XP_006711988.1:p.Phe949Tyr
XM_011532489.1:c.2903T>A	XP_011530791.1:p.Phe968Tyr
XM_011532490.1:c.2900T>A	XP_011530792.1:p.Phe967Tyr
XM_011532491.1:c.2837T>A	XP_011530793.1:p.Phe946Tyr
XM_011532492.1:c.2903T>A	XP_011530794.1:p.Phe968Tyr
XM_011532493.1:c.2765T>A	XP_011530795.1:p.Phe922Tyr
XM_011532494.1:c.2705T>A	XP_011530796.1:p.Phe902Tyr
XM_011532495.1:c.2237T>A	XP_011530797.1:p.Phe746Tyr
XM_011532496.1:c.2180T>A	XP_011530798.1:p.Phe727Tyr
NM_001320613.1:c.2780T>A	NP_001307542.1:p.Phe927Tyr
NM_004036.4:c.2777T>A	NP_004027.2:p.Phe926Tyr
XM_011532492.2:c.2903T>A	XP_011530794.1:p.Phe968Tyr
XM_017003186.1:c.2843T>A	XP_016858675.1:p.Phe948Tyr
XM_017003187.1:c.2834T>A	XP_016858676.1:p.Phe945Tyr
XM_017003188.1:c.2900T>A	XP_016858677.1:p.Phe967Tyr
XM_017003189.1:c.2762T>A	XP_016858678.1:p.Phe921Tyr
XM_017003190.1:c.2639T>A	XP_016858679.1:p.Phe880Tyr
XM_017003191.1:c.2267T>A	XP_016858680.1:p.Phe756Tyr
XM_017003192.1:c.2057T>A	XP_016858681.1:p.Phe686Tyr
XM_017003193.1:c.2054T>A	XP_016858682.1:p.Phe685Tyr
NM_001320613.2:c.2780T>A	NP_001307542.1:p.Phe927Tyr
NM_001377128.1:c.2843T>A	NP_001364057.1:p.Phe948Tyr
NM_001377129.1:c.2639T>A	NP_001364058.1:p.Phe880Tyr
NM_001377130.1:c.2332-685T>A	NP_001364059.1:n.2332-685T>A
NM_001377131.1:c.2054T>A	NP_001364060.1:p.Phe685Tyr
NM_001377132.1:c.2777T>A	NP_001364061.1:p.Phe926Tyr
NM_004036.5:c.2777T>A MANE Select	NP_004027.2:p.Phe926Tyr