Canonical Allele Identifier: CA346062564

Gene: ADCY3

Linked Data

• dbSNP Id: rs2148371261
• gnomAD v3: 2-24823244-G-A
• gnomAD v4: 2-24823244-G-A
• MyVariant Identifiers: chr2:g.25046113G>A (hg19) ; chr2:g.24823244G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823244G>A , CM000664.2:g.24823244G>A	GRCh38
NC_000002.11:g.25046113G>A , CM000664.1:g.25046113G>A	GRCh37
NC_000002.10:g.24899617G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2851C>T	ENSP00000384484.2:p.Arg951Cys
ENST00000679454.1:c.2848C>T MANE Select	ENSP00000505261.1:p.Arg950Cys
ENST00000260600.9:c.2848C>T	ENSP00000260600.5:p.Arg950Cys
ENST00000405392.5:c.2851C>T	ENSP00000384484.2:p.Arg951Cys
ENST00000485887.1:n.120C>T
ENST00000606682.5:c.1789C>T	ENSP00000475652.1:p.Arg597Cys
NM_004036.3:c.2848C>T	NP_004027.2:p.Arg950Cys
XM_005264104.1:c.2851C>T	XP_005264161.1:p.Arg951Cys
XM_005264105.1:c.2848C>T	XP_005264162.1:p.Arg950Cys
XM_006711925.1:c.2917C>T	XP_006711988.1:p.Arg973Cys
XM_011532489.1:c.2974C>T	XP_011530791.1:p.Arg992Cys
XM_011532490.1:c.2971C>T	XP_011530792.1:p.Arg991Cys
XM_011532491.1:c.2908C>T	XP_011530793.1:p.Arg970Cys
XM_011532492.1:c.2974C>T	XP_011530794.1:p.Arg992Cys
XM_011532493.1:c.2836C>T	XP_011530795.1:p.Arg946Cys
XM_011532494.1:c.2776C>T	XP_011530796.1:p.Arg926Cys
XM_011532495.1:c.2308C>T	XP_011530797.1:p.Arg770Cys
XM_011532496.1:c.2251C>T	XP_011530798.1:p.Arg751Cys
NM_001320613.1:c.2851C>T	NP_001307542.1:p.Arg951Cys
NM_004036.4:c.2848C>T	NP_004027.2:p.Arg950Cys
XM_011532492.2:c.2974C>T	XP_011530794.1:p.Arg992Cys
XM_017003186.1:c.2914C>T	XP_016858675.1:p.Arg972Cys
XM_017003187.1:c.2905C>T	XP_016858676.1:p.Arg969Cys
XM_017003188.1:c.2971C>T	XP_016858677.1:p.Arg991Cys
XM_017003189.1:c.2833C>T	XP_016858678.1:p.Arg945Cys
XM_017003190.1:c.2710C>T	XP_016858679.1:p.Arg904Cys
XM_017003191.1:c.2338C>T	XP_016858680.1:p.Arg780Cys
XM_017003192.1:c.2128C>T	XP_016858681.1:p.Arg710Cys
XM_017003193.1:c.2125C>T	XP_016858682.1:p.Arg709Cys
NM_001320613.2:c.2851C>T	NP_001307542.1:p.Arg951Cys
NM_001377128.1:c.2914C>T	NP_001364057.1:p.Arg972Cys
NM_001377129.1:c.2710C>T	NP_001364058.1:p.Arg904Cys
NM_001377130.1:c.2332-614C>T	NP_001364059.1:n.2332-614C>T
NM_001377131.1:c.2125C>T	NP_001364060.1:p.Arg709Cys
NM_001377132.1:c.2848C>T	NP_001364061.1:p.Arg950Cys
NM_004036.5:c.2848C>T MANE Select	NP_004027.2:p.Arg950Cys