Canonical Allele Identifier: CA346062640

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046128C>G (hg19) ; chr2:g.24823259C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823259C>G , CM000664.2:g.24823259C>G	GRCh38
NC_000002.11:g.25046128C>G , CM000664.1:g.25046128C>G	GRCh37
NC_000002.10:g.24899632C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2836G>C	ENSP00000384484.2:p.Gly946Arg
ENST00000679454.1:c.2833G>C MANE Select	ENSP00000505261.1:p.Gly945Arg
ENST00000260600.9:c.2833G>C	ENSP00000260600.5:p.Gly945Arg
ENST00000405392.5:c.2836G>C	ENSP00000384484.2:p.Gly946Arg
ENST00000485887.1:n.105G>C
ENST00000606682.5:c.1774G>C	ENSP00000475652.1:p.Gly592Arg
NM_004036.3:c.2833G>C	NP_004027.2:p.Gly945Arg
XM_005264104.1:c.2836G>C	XP_005264161.1:p.Gly946Arg
XM_005264105.1:c.2833G>C	XP_005264162.1:p.Gly945Arg
XM_006711925.1:c.2902G>C	XP_006711988.1:p.Gly968Arg
XM_011532489.1:c.2959G>C	XP_011530791.1:p.Gly987Arg
XM_011532490.1:c.2956G>C	XP_011530792.1:p.Gly986Arg
XM_011532491.1:c.2893G>C	XP_011530793.1:p.Gly965Arg
XM_011532492.1:c.2959G>C	XP_011530794.1:p.Gly987Arg
XM_011532493.1:c.2821G>C	XP_011530795.1:p.Gly941Arg
XM_011532494.1:c.2761G>C	XP_011530796.1:p.Gly921Arg
XM_011532495.1:c.2293G>C	XP_011530797.1:p.Gly765Arg
XM_011532496.1:c.2236G>C	XP_011530798.1:p.Gly746Arg
NM_001320613.1:c.2836G>C	NP_001307542.1:p.Gly946Arg
NM_004036.4:c.2833G>C	NP_004027.2:p.Gly945Arg
XM_011532492.2:c.2959G>C	XP_011530794.1:p.Gly987Arg
XM_017003186.1:c.2899G>C	XP_016858675.1:p.Gly967Arg
XM_017003187.1:c.2890G>C	XP_016858676.1:p.Gly964Arg
XM_017003188.1:c.2956G>C	XP_016858677.1:p.Gly986Arg
XM_017003189.1:c.2818G>C	XP_016858678.1:p.Gly940Arg
XM_017003190.1:c.2695G>C	XP_016858679.1:p.Gly899Arg
XM_017003191.1:c.2323G>C	XP_016858680.1:p.Gly775Arg
XM_017003192.1:c.2113G>C	XP_016858681.1:p.Gly705Arg
XM_017003193.1:c.2110G>C	XP_016858682.1:p.Gly704Arg
NM_001320613.2:c.2836G>C	NP_001307542.1:p.Gly946Arg
NM_001377128.1:c.2899G>C	NP_001364057.1:p.Gly967Arg
NM_001377129.1:c.2695G>C	NP_001364058.1:p.Gly899Arg
NM_001377130.1:c.2332-629G>C	NP_001364059.1:n.2332-629G>C
NM_001377131.1:c.2110G>C	NP_001364060.1:p.Gly704Arg
NM_001377132.1:c.2833G>C	NP_001364061.1:p.Gly945Arg
NM_004036.5:c.2833G>C MANE Select	NP_004027.2:p.Gly945Arg