Canonical Allele Identifier: CA425172011

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046183A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823314A>G , CM000664.2:g.24823314A>G	GRCh38
NC_000002.11:g.25046183A>G , CM000664.1:g.25046183A>G	GRCh37
NC_000002.10:g.24899687A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2781T>C	ENSP00000384484.2:p.Phe927=
ENST00000679454.1:c.2778T>C MANE Select	ENSP00000505261.1:p.Phe926=
ENST00000260600.9:c.2778T>C	ENSP00000260600.5:p.Phe926=
ENST00000405392.5:c.2781T>C	ENSP00000384484.2:p.Phe927=
ENST00000485887.1:n.50T>C
ENST00000606682.5:c.1719T>C	ENSP00000475652.1:p.Phe573=
NM_004036.3:c.2778T>C	NP_004027.2:p.Phe926=
XM_005264104.1:c.2781T>C	XP_005264161.1:p.Phe927=
XM_005264105.1:c.2778T>C	XP_005264162.1:p.Phe926=
XM_006711925.1:c.2847T>C	XP_006711988.1:p.Phe949=
XM_011532489.1:c.2904T>C	XP_011530791.1:p.Phe968=
XM_011532490.1:c.2901T>C	XP_011530792.1:p.Phe967=
XM_011532491.1:c.2838T>C	XP_011530793.1:p.Phe946=
XM_011532492.1:c.2904T>C	XP_011530794.1:p.Phe968=
XM_011532493.1:c.2766T>C	XP_011530795.1:p.Phe922=
XM_011532494.1:c.2706T>C	XP_011530796.1:p.Phe902=
XM_011532495.1:c.2238T>C	XP_011530797.1:p.Phe746=
XM_011532496.1:c.2181T>C	XP_011530798.1:p.Phe727=
NM_001320613.1:c.2781T>C	NP_001307542.1:p.Phe927=
NM_004036.4:c.2778T>C	NP_004027.2:p.Phe926=
XM_011532492.2:c.2904T>C	XP_011530794.1:p.Phe968=
XM_017003186.1:c.2844T>C	XP_016858675.1:p.Phe948=
XM_017003187.1:c.2835T>C	XP_016858676.1:p.Phe945=
XM_017003188.1:c.2901T>C	XP_016858677.1:p.Phe967=
XM_017003189.1:c.2763T>C	XP_016858678.1:p.Phe921=
XM_017003190.1:c.2640T>C	XP_016858679.1:p.Phe880=
XM_017003191.1:c.2268T>C	XP_016858680.1:p.Phe756=
XM_017003192.1:c.2058T>C	XP_016858681.1:p.Phe686=
XM_017003193.1:c.2055T>C	XP_016858682.1:p.Phe685=
NM_001320613.2:c.2781T>C	NP_001307542.1:p.Phe927=
NM_001377128.1:c.2844T>C	NP_001364057.1:p.Phe948=
NM_001377129.1:c.2640T>C	NP_001364058.1:p.Phe880=
NM_001377130.1:c.2332-684T>C	NP_001364059.1:n.2332-684T>C
NM_001377131.1:c.2055T>C	NP_001364060.1:p.Phe685=
NM_001377132.1:c.2778T>C	NP_001364061.1:p.Phe926=
NM_004036.5:c.2778T>C MANE Select	NP_004027.2:p.Phe926=