Canonical Allele Identifier: CA346062654

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046131C>A (hg19) ; chr2:g.24823262C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823262C>A , CM000664.2:g.24823262C>A	GRCh38
NC_000002.11:g.25046131C>A , CM000664.1:g.25046131C>A	GRCh37
NC_000002.10:g.24899635C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2833G>T	ENSP00000384484.2:p.Gly945Cys
ENST00000679454.1:c.2830G>T MANE Select	ENSP00000505261.1:p.Gly944Cys
ENST00000260600.9:c.2830G>T	ENSP00000260600.5:p.Gly944Cys
ENST00000405392.5:c.2833G>T	ENSP00000384484.2:p.Gly945Cys
ENST00000485887.1:n.102G>T
ENST00000606682.5:c.1771G>T	ENSP00000475652.1:p.Gly591Cys
NM_004036.3:c.2830G>T	NP_004027.2:p.Gly944Cys
XM_005264104.1:c.2833G>T	XP_005264161.1:p.Gly945Cys
XM_005264105.1:c.2830G>T	XP_005264162.1:p.Gly944Cys
XM_006711925.1:c.2899G>T	XP_006711988.1:p.Gly967Cys
XM_011532489.1:c.2956G>T	XP_011530791.1:p.Gly986Cys
XM_011532490.1:c.2953G>T	XP_011530792.1:p.Gly985Cys
XM_011532491.1:c.2890G>T	XP_011530793.1:p.Gly964Cys
XM_011532492.1:c.2956G>T	XP_011530794.1:p.Gly986Cys
XM_011532493.1:c.2818G>T	XP_011530795.1:p.Gly940Cys
XM_011532494.1:c.2758G>T	XP_011530796.1:p.Gly920Cys
XM_011532495.1:c.2290G>T	XP_011530797.1:p.Gly764Cys
XM_011532496.1:c.2233G>T	XP_011530798.1:p.Gly745Cys
NM_001320613.1:c.2833G>T	NP_001307542.1:p.Gly945Cys
NM_004036.4:c.2830G>T	NP_004027.2:p.Gly944Cys
XM_011532492.2:c.2956G>T	XP_011530794.1:p.Gly986Cys
XM_017003186.1:c.2896G>T	XP_016858675.1:p.Gly966Cys
XM_017003187.1:c.2887G>T	XP_016858676.1:p.Gly963Cys
XM_017003188.1:c.2953G>T	XP_016858677.1:p.Gly985Cys
XM_017003189.1:c.2815G>T	XP_016858678.1:p.Gly939Cys
XM_017003190.1:c.2692G>T	XP_016858679.1:p.Gly898Cys
XM_017003191.1:c.2320G>T	XP_016858680.1:p.Gly774Cys
XM_017003192.1:c.2110G>T	XP_016858681.1:p.Gly704Cys
XM_017003193.1:c.2107G>T	XP_016858682.1:p.Gly703Cys
NM_001320613.2:c.2833G>T	NP_001307542.1:p.Gly945Cys
NM_001377128.1:c.2896G>T	NP_001364057.1:p.Gly966Cys
NM_001377129.1:c.2692G>T	NP_001364058.1:p.Gly898Cys
NM_001377130.1:c.2332-632G>T	NP_001364059.1:n.2332-632G>T
NM_001377131.1:c.2107G>T	NP_001364060.1:p.Gly703Cys
NM_001377132.1:c.2830G>T	NP_001364061.1:p.Gly944Cys
NM_004036.5:c.2830G>T MANE Select	NP_004027.2:p.Gly944Cys