Canonical Allele Identifier: CA346062517

Gene: ADCY3

Linked Data

• COSMIC: COSM1019189
• MyVariant Identifiers: chr2:g.25046099T>A (hg19) ; chr2:g.24823230T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823230T>A , CM000664.2:g.24823230T>A	GRCh38
NC_000002.11:g.25046099T>A , CM000664.1:g.25046099T>A	GRCh37
NC_000002.10:g.24899603T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2865A>T	ENSP00000384484.2:p.Glu955Asp
ENST00000679454.1:c.2862A>T MANE Select	ENSP00000505261.1:p.Glu954Asp
ENST00000260600.9:c.2862A>T	ENSP00000260600.5:p.Glu954Asp
ENST00000405392.5:c.2865A>T	ENSP00000384484.2:p.Glu955Asp
ENST00000485887.1:n.134A>T
ENST00000606682.5:c.1803A>T	ENSP00000475652.1:p.Glu601Asp
NM_004036.3:c.2862A>T	NP_004027.2:p.Glu954Asp
XM_005264104.1:c.2865A>T	XP_005264161.1:p.Glu955Asp
XM_005264105.1:c.2862A>T	XP_005264162.1:p.Glu954Asp
XM_006711925.1:c.2931A>T	XP_006711988.1:p.Glu977Asp
XM_011532489.1:c.2988A>T	XP_011530791.1:p.Glu996Asp
XM_011532490.1:c.2985A>T	XP_011530792.1:p.Glu995Asp
XM_011532491.1:c.2922A>T	XP_011530793.1:p.Glu974Asp
XM_011532492.1:c.2988A>T	XP_011530794.1:p.Glu996Asp
XM_011532493.1:c.2850A>T	XP_011530795.1:p.Glu950Asp
XM_011532494.1:c.2790A>T	XP_011530796.1:p.Glu930Asp
XM_011532495.1:c.2322A>T	XP_011530797.1:p.Glu774Asp
XM_011532496.1:c.2265A>T	XP_011530798.1:p.Glu755Asp
NM_001320613.1:c.2865A>T	NP_001307542.1:p.Glu955Asp
NM_004036.4:c.2862A>T	NP_004027.2:p.Glu954Asp
XM_011532492.2:c.2988A>T	XP_011530794.1:p.Glu996Asp
XM_017003186.1:c.2928A>T	XP_016858675.1:p.Glu976Asp
XM_017003187.1:c.2919A>T	XP_016858676.1:p.Glu973Asp
XM_017003188.1:c.2985A>T	XP_016858677.1:p.Glu995Asp
XM_017003189.1:c.2847A>T	XP_016858678.1:p.Glu949Asp
XM_017003190.1:c.2724A>T	XP_016858679.1:p.Glu908Asp
XM_017003191.1:c.2352A>T	XP_016858680.1:p.Glu784Asp
XM_017003192.1:c.2142A>T	XP_016858681.1:p.Glu714Asp
XM_017003193.1:c.2139A>T	XP_016858682.1:p.Glu713Asp
NM_001320613.2:c.2865A>T	NP_001307542.1:p.Glu955Asp
NM_001377128.1:c.2928A>T	NP_001364057.1:p.Glu976Asp
NM_001377129.1:c.2724A>T	NP_001364058.1:p.Glu908Asp
NM_001377130.1:c.2332-600A>T	NP_001364059.1:n.2332-600A>T
NM_001377131.1:c.2139A>T	NP_001364060.1:p.Glu713Asp
NM_001377132.1:c.2862A>T	NP_001364061.1:p.Glu954Asp
NM_004036.5:c.2862A>T MANE Select	NP_004027.2:p.Glu954Asp