Canonical Allele Identifier: CA346063000

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046198C>A (hg19) ; chr2:g.24823329C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823329C>A , CM000664.2:g.24823329C>A	GRCh38
NC_000002.11:g.25046198C>A , CM000664.1:g.25046198C>A	GRCh37
NC_000002.10:g.24899702C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2766G>T	ENSP00000384484.2:p.Glu922Asp
ENST00000679454.1:c.2763G>T MANE Select	ENSP00000505261.1:p.Glu921Asp
ENST00000260600.9:c.2763G>T	ENSP00000260600.5:p.Glu921Asp
ENST00000405392.5:c.2766G>T	ENSP00000384484.2:p.Glu922Asp
ENST00000485887.1:n.35G>T
ENST00000606682.5:c.1704G>T	ENSP00000475652.1:p.Glu568Asp
NM_004036.3:c.2763G>T	NP_004027.2:p.Glu921Asp
XM_005264104.1:c.2766G>T	XP_005264161.1:p.Glu922Asp
XM_005264105.1:c.2763G>T	XP_005264162.1:p.Glu921Asp
XM_006711925.1:c.2832G>T	XP_006711988.1:p.Glu944Asp
XM_011532489.1:c.2889G>T	XP_011530791.1:p.Glu963Asp
XM_011532490.1:c.2886G>T	XP_011530792.1:p.Glu962Asp
XM_011532491.1:c.2823G>T	XP_011530793.1:p.Glu941Asp
XM_011532492.1:c.2889G>T	XP_011530794.1:p.Glu963Asp
XM_011532493.1:c.2751G>T	XP_011530795.1:p.Glu917Asp
XM_011532494.1:c.2691G>T	XP_011530796.1:p.Glu897Asp
XM_011532495.1:c.2223G>T	XP_011530797.1:p.Glu741Asp
XM_011532496.1:c.2166G>T	XP_011530798.1:p.Glu722Asp
NM_001320613.1:c.2766G>T	NP_001307542.1:p.Glu922Asp
NM_004036.4:c.2763G>T	NP_004027.2:p.Glu921Asp
XM_011532492.2:c.2889G>T	XP_011530794.1:p.Glu963Asp
XM_017003186.1:c.2829G>T	XP_016858675.1:p.Glu943Asp
XM_017003187.1:c.2820G>T	XP_016858676.1:p.Glu940Asp
XM_017003188.1:c.2886G>T	XP_016858677.1:p.Glu962Asp
XM_017003189.1:c.2748G>T	XP_016858678.1:p.Glu916Asp
XM_017003190.1:c.2625G>T	XP_016858679.1:p.Glu875Asp
XM_017003191.1:c.2253G>T	XP_016858680.1:p.Glu751Asp
XM_017003192.1:c.2043G>T	XP_016858681.1:p.Glu681Asp
XM_017003193.1:c.2040G>T	XP_016858682.1:p.Glu680Asp
NM_001320613.2:c.2766G>T	NP_001307542.1:p.Glu922Asp
NM_001377128.1:c.2829G>T	NP_001364057.1:p.Glu943Asp
NM_001377129.1:c.2625G>T	NP_001364058.1:p.Glu875Asp
NM_001377130.1:c.2332-699G>T	NP_001364059.1:n.2332-699G>T
NM_001377131.1:c.2040G>T	NP_001364060.1:p.Glu680Asp
NM_001377132.1:c.2763G>T	NP_001364061.1:p.Glu921Asp
NM_004036.5:c.2763G>T MANE Select	NP_004027.2:p.Glu921Asp