Canonical Allele Identifier: CA346062987

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046196A>C (hg19) ; chr2:g.24823327A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823327A>C , CM000664.2:g.24823327A>C	GRCh38
NC_000002.11:g.25046196A>C , CM000664.1:g.25046196A>C	GRCh37
NC_000002.10:g.24899700A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2768T>G	ENSP00000384484.2:p.Ile923Ser
ENST00000679454.1:c.2765T>G MANE Select	ENSP00000505261.1:p.Ile922Ser
ENST00000260600.9:c.2765T>G	ENSP00000260600.5:p.Ile922Ser
ENST00000405392.5:c.2768T>G	ENSP00000384484.2:p.Ile923Ser
ENST00000485887.1:n.37T>G
ENST00000606682.5:c.1706T>G	ENSP00000475652.1:p.Ile569Ser
NM_004036.3:c.2765T>G	NP_004027.2:p.Ile922Ser
XM_005264104.1:c.2768T>G	XP_005264161.1:p.Ile923Ser
XM_005264105.1:c.2765T>G	XP_005264162.1:p.Ile922Ser
XM_006711925.1:c.2834T>G	XP_006711988.1:p.Ile945Ser
XM_011532489.1:c.2891T>G	XP_011530791.1:p.Ile964Ser
XM_011532490.1:c.2888T>G	XP_011530792.1:p.Ile963Ser
XM_011532491.1:c.2825T>G	XP_011530793.1:p.Ile942Ser
XM_011532492.1:c.2891T>G	XP_011530794.1:p.Ile964Ser
XM_011532493.1:c.2753T>G	XP_011530795.1:p.Ile918Ser
XM_011532494.1:c.2693T>G	XP_011530796.1:p.Ile898Ser
XM_011532495.1:c.2225T>G	XP_011530797.1:p.Ile742Ser
XM_011532496.1:c.2168T>G	XP_011530798.1:p.Ile723Ser
NM_001320613.1:c.2768T>G	NP_001307542.1:p.Ile923Ser
NM_004036.4:c.2765T>G	NP_004027.2:p.Ile922Ser
XM_011532492.2:c.2891T>G	XP_011530794.1:p.Ile964Ser
XM_017003186.1:c.2831T>G	XP_016858675.1:p.Ile944Ser
XM_017003187.1:c.2822T>G	XP_016858676.1:p.Ile941Ser
XM_017003188.1:c.2888T>G	XP_016858677.1:p.Ile963Ser
XM_017003189.1:c.2750T>G	XP_016858678.1:p.Ile917Ser
XM_017003190.1:c.2627T>G	XP_016858679.1:p.Ile876Ser
XM_017003191.1:c.2255T>G	XP_016858680.1:p.Ile752Ser
XM_017003192.1:c.2045T>G	XP_016858681.1:p.Ile682Ser
XM_017003193.1:c.2042T>G	XP_016858682.1:p.Ile681Ser
NM_001320613.2:c.2768T>G	NP_001307542.1:p.Ile923Ser
NM_001377128.1:c.2831T>G	NP_001364057.1:p.Ile944Ser
NM_001377129.1:c.2627T>G	NP_001364058.1:p.Ile876Ser
NM_001377130.1:c.2332-697T>G	NP_001364059.1:n.2332-697T>G
NM_001377131.1:c.2042T>G	NP_001364060.1:p.Ile681Ser
NM_001377132.1:c.2765T>G	NP_001364061.1:p.Ile922Ser
NM_004036.5:c.2765T>G MANE Select	NP_004027.2:p.Ile922Ser