Canonical Allele Identifier: CA425171957

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046111A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823242A>C , CM000664.2:g.24823242A>C	GRCh38
NC_000002.11:g.25046111A>C , CM000664.1:g.25046111A>C	GRCh37
NC_000002.10:g.24899615A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2853T>G	ENSP00000384484.2:p.Arg951=
ENST00000679454.1:c.2850T>G MANE Select	ENSP00000505261.1:p.Arg950=
ENST00000260600.9:c.2850T>G	ENSP00000260600.5:p.Arg950=
ENST00000405392.5:c.2853T>G	ENSP00000384484.2:p.Arg951=
ENST00000485887.1:n.122T>G
ENST00000606682.5:c.1791T>G	ENSP00000475652.1:p.Arg597=
NM_004036.3:c.2850T>G	NP_004027.2:p.Arg950=
XM_005264104.1:c.2853T>G	XP_005264161.1:p.Arg951=
XM_005264105.1:c.2850T>G	XP_005264162.1:p.Arg950=
XM_006711925.1:c.2919T>G	XP_006711988.1:p.Arg973=
XM_011532489.1:c.2976T>G	XP_011530791.1:p.Arg992=
XM_011532490.1:c.2973T>G	XP_011530792.1:p.Arg991=
XM_011532491.1:c.2910T>G	XP_011530793.1:p.Arg970=
XM_011532492.1:c.2976T>G	XP_011530794.1:p.Arg992=
XM_011532493.1:c.2838T>G	XP_011530795.1:p.Arg946=
XM_011532494.1:c.2778T>G	XP_011530796.1:p.Arg926=
XM_011532495.1:c.2310T>G	XP_011530797.1:p.Arg770=
XM_011532496.1:c.2253T>G	XP_011530798.1:p.Arg751=
NM_001320613.1:c.2853T>G	NP_001307542.1:p.Arg951=
NM_004036.4:c.2850T>G	NP_004027.2:p.Arg950=
XM_011532492.2:c.2976T>G	XP_011530794.1:p.Arg992=
XM_017003186.1:c.2916T>G	XP_016858675.1:p.Arg972=
XM_017003187.1:c.2907T>G	XP_016858676.1:p.Arg969=
XM_017003188.1:c.2973T>G	XP_016858677.1:p.Arg991=
XM_017003189.1:c.2835T>G	XP_016858678.1:p.Arg945=
XM_017003190.1:c.2712T>G	XP_016858679.1:p.Arg904=
XM_017003191.1:c.2340T>G	XP_016858680.1:p.Arg780=
XM_017003192.1:c.2130T>G	XP_016858681.1:p.Arg710=
XM_017003193.1:c.2127T>G	XP_016858682.1:p.Arg709=
NM_001320613.2:c.2853T>G	NP_001307542.1:p.Arg951=
NM_001377128.1:c.2916T>G	NP_001364057.1:p.Arg972=
NM_001377129.1:c.2712T>G	NP_001364058.1:p.Arg904=
NM_001377130.1:c.2332-612T>G	NP_001364059.1:n.2332-612T>G
NM_001377131.1:c.2127T>G	NP_001364060.1:p.Arg709=
NM_001377132.1:c.2850T>G	NP_001364061.1:p.Arg950=
NM_004036.5:c.2850T>G MANE Select	NP_004027.2:p.Arg950=