Canonical Allele Identifier: CA425171982

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24823260-A-C
• MyVariant Identifiers: chr2:g.25046129A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823260A>C , CM000664.2:g.24823260A>C	GRCh38
NC_000002.11:g.25046129A>C , CM000664.1:g.25046129A>C	GRCh37
NC_000002.10:g.24899633A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2835T>G	ENSP00000384484.2:p.Gly945=
ENST00000679454.1:c.2832T>G MANE Select	ENSP00000505261.1:p.Gly944=
ENST00000260600.9:c.2832T>G	ENSP00000260600.5:p.Gly944=
ENST00000405392.5:c.2835T>G	ENSP00000384484.2:p.Gly945=
ENST00000485887.1:n.104T>G
ENST00000606682.5:c.1773T>G	ENSP00000475652.1:p.Gly591=
NM_004036.3:c.2832T>G	NP_004027.2:p.Gly944=
XM_005264104.1:c.2835T>G	XP_005264161.1:p.Gly945=
XM_005264105.1:c.2832T>G	XP_005264162.1:p.Gly944=
XM_006711925.1:c.2901T>G	XP_006711988.1:p.Gly967=
XM_011532489.1:c.2958T>G	XP_011530791.1:p.Gly986=
XM_011532490.1:c.2955T>G	XP_011530792.1:p.Gly985=
XM_011532491.1:c.2892T>G	XP_011530793.1:p.Gly964=
XM_011532492.1:c.2958T>G	XP_011530794.1:p.Gly986=
XM_011532493.1:c.2820T>G	XP_011530795.1:p.Gly940=
XM_011532494.1:c.2760T>G	XP_011530796.1:p.Gly920=
XM_011532495.1:c.2292T>G	XP_011530797.1:p.Gly764=
XM_011532496.1:c.2235T>G	XP_011530798.1:p.Gly745=
NM_001320613.1:c.2835T>G	NP_001307542.1:p.Gly945=
NM_004036.4:c.2832T>G	NP_004027.2:p.Gly944=
XM_011532492.2:c.2958T>G	XP_011530794.1:p.Gly986=
XM_017003186.1:c.2898T>G	XP_016858675.1:p.Gly966=
XM_017003187.1:c.2889T>G	XP_016858676.1:p.Gly963=
XM_017003188.1:c.2955T>G	XP_016858677.1:p.Gly985=
XM_017003189.1:c.2817T>G	XP_016858678.1:p.Gly939=
XM_017003190.1:c.2694T>G	XP_016858679.1:p.Gly898=
XM_017003191.1:c.2322T>G	XP_016858680.1:p.Gly774=
XM_017003192.1:c.2112T>G	XP_016858681.1:p.Gly704=
XM_017003193.1:c.2109T>G	XP_016858682.1:p.Gly703=
NM_001320613.2:c.2835T>G	NP_001307542.1:p.Gly945=
NM_001377128.1:c.2898T>G	NP_001364057.1:p.Gly966=
NM_001377129.1:c.2694T>G	NP_001364058.1:p.Gly898=
NM_001377130.1:c.2332-630T>G	NP_001364059.1:n.2332-630T>G
NM_001377131.1:c.2109T>G	NP_001364060.1:p.Gly703=
NM_001377132.1:c.2832T>G	NP_001364061.1:p.Gly944=
NM_004036.5:c.2832T>G MANE Select	NP_004027.2:p.Gly944=