Canonical Allele Identifier: CA346063677

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047334C>A (hg19) ; chr2:g.24824465C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824465C>A , CM000664.2:g.24824465C>A	GRCh38
NC_000002.11:g.25047334C>A , CM000664.1:g.25047334C>A	GRCh37
NC_000002.10:g.24900838C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2652G>T	ENSP00000384484.2:p.Glu884Asp
ENST00000679454.1:c.2649G>T MANE Select	ENSP00000505261.1:p.Glu883Asp
ENST00000260600.9:c.2649G>T	ENSP00000260600.5:p.Glu883Asp
ENST00000405392.5:c.2652G>T	ENSP00000384484.2:p.Glu884Asp
ENST00000606682.5:c.1590G>T	ENSP00000475652.1:p.Glu530Asp
NM_004036.3:c.2649G>T	NP_004027.2:p.Glu883Asp
XM_005264104.1:c.2652G>T	XP_005264161.1:p.Glu884Asp
XM_005264105.1:c.2649G>T	XP_005264162.1:p.Glu883Asp
XM_006711925.1:c.2718G>T	XP_006711988.1:p.Glu906Asp
XM_011532489.1:c.2775G>T	XP_011530791.1:p.Glu925Asp
XM_011532490.1:c.2772G>T	XP_011530792.1:p.Glu924Asp
XM_011532491.1:c.2709G>T	XP_011530793.1:p.Glu903Asp
XM_011532492.1:c.2775G>T	XP_011530794.1:p.Glu925Asp
XM_011532493.1:c.2637G>T	XP_011530795.1:p.Glu879Asp
XM_011532494.1:c.2577G>T	XP_011530796.1:p.Glu859Asp
XM_011532495.1:c.2109G>T	XP_011530797.1:p.Glu703Asp
XM_011532496.1:c.2052G>T	XP_011530798.1:p.Glu684Asp
NM_001320613.1:c.2652G>T	NP_001307542.1:p.Glu884Asp
NM_004036.4:c.2649G>T	NP_004027.2:p.Glu883Asp
XM_011532492.2:c.2775G>T	XP_011530794.1:p.Glu925Asp
XM_017003186.1:c.2715G>T	XP_016858675.1:p.Glu905Asp
XM_017003187.1:c.2706G>T	XP_016858676.1:p.Glu902Asp
XM_017003188.1:c.2772G>T	XP_016858677.1:p.Glu924Asp
XM_017003189.1:c.2634G>T	XP_016858678.1:p.Glu878Asp
XM_017003190.1:c.2511G>T	XP_016858679.1:p.Glu837Asp
XM_017003191.1:c.2139G>T	XP_016858680.1:p.Glu713Asp
XM_017003192.1:c.1929G>T	XP_016858681.1:p.Glu643Asp
XM_017003193.1:c.1926G>T	XP_016858682.1:p.Glu642Asp
NM_001320613.2:c.2652G>T	NP_001307542.1:p.Glu884Asp
NM_001377128.1:c.2715G>T	NP_001364057.1:p.Glu905Asp
NM_001377129.1:c.2511G>T	NP_001364058.1:p.Glu837Asp
NM_001377130.1:c.2244G>T	NP_001364059.1:p.Glu748Asp
NM_001377131.1:c.1926G>T	NP_001364060.1:p.Glu642Asp
NM_001377132.1:c.2649G>T	NP_001364061.1:p.Glu883Asp
NM_004036.5:c.2649G>T MANE Select	NP_004027.2:p.Glu883Asp