Canonical Allele Identifier: CA346062938

Gene: ADCY3

Linked Data

• dbSNP Id: rs1221967443
• gnomAD v2: 2-25046181-G-A
• MyVariant Identifiers: chr2:g.25046181G>A (hg19) ; chr2:g.24823312G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823312G>A , CM000664.2:g.24823312G>A	GRCh38
NC_000002.11:g.25046181G>A , CM000664.1:g.25046181G>A	GRCh37
NC_000002.10:g.24899685G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2783C>T	ENSP00000384484.2:p.Ala928Val
ENST00000679454.1:c.2780C>T MANE Select	ENSP00000505261.1:p.Ala927Val
ENST00000260600.9:c.2780C>T	ENSP00000260600.5:p.Ala927Val
ENST00000405392.5:c.2783C>T	ENSP00000384484.2:p.Ala928Val
ENST00000485887.1:n.52C>T
ENST00000606682.5:c.1721C>T	ENSP00000475652.1:p.Ala574Val
NM_004036.3:c.2780C>T	NP_004027.2:p.Ala927Val
XM_005264104.1:c.2783C>T	XP_005264161.1:p.Ala928Val
XM_005264105.1:c.2780C>T	XP_005264162.1:p.Ala927Val
XM_006711925.1:c.2849C>T	XP_006711988.1:p.Ala950Val
XM_011532489.1:c.2906C>T	XP_011530791.1:p.Ala969Val
XM_011532490.1:c.2903C>T	XP_011530792.1:p.Ala968Val
XM_011532491.1:c.2840C>T	XP_011530793.1:p.Ala947Val
XM_011532492.1:c.2906C>T	XP_011530794.1:p.Ala969Val
XM_011532493.1:c.2768C>T	XP_011530795.1:p.Ala923Val
XM_011532494.1:c.2708C>T	XP_011530796.1:p.Ala903Val
XM_011532495.1:c.2240C>T	XP_011530797.1:p.Ala747Val
XM_011532496.1:c.2183C>T	XP_011530798.1:p.Ala728Val
NM_001320613.1:c.2783C>T	NP_001307542.1:p.Ala928Val
NM_004036.4:c.2780C>T	NP_004027.2:p.Ala927Val
XM_011532492.2:c.2906C>T	XP_011530794.1:p.Ala969Val
XM_017003186.1:c.2846C>T	XP_016858675.1:p.Ala949Val
XM_017003187.1:c.2837C>T	XP_016858676.1:p.Ala946Val
XM_017003188.1:c.2903C>T	XP_016858677.1:p.Ala968Val
XM_017003189.1:c.2765C>T	XP_016858678.1:p.Ala922Val
XM_017003190.1:c.2642C>T	XP_016858679.1:p.Ala881Val
XM_017003191.1:c.2270C>T	XP_016858680.1:p.Ala757Val
XM_017003192.1:c.2060C>T	XP_016858681.1:p.Ala687Val
XM_017003193.1:c.2057C>T	XP_016858682.1:p.Ala686Val
NM_001320613.2:c.2783C>T	NP_001307542.1:p.Ala928Val
NM_001377128.1:c.2846C>T	NP_001364057.1:p.Ala949Val
NM_001377129.1:c.2642C>T	NP_001364058.1:p.Ala881Val
NM_001377130.1:c.2332-682C>T	NP_001364059.1:n.2332-682C>T
NM_001377131.1:c.2057C>T	NP_001364060.1:p.Ala686Val
NM_001377132.1:c.2780C>T	NP_001364061.1:p.Ala927Val
NM_004036.5:c.2780C>T MANE Select	NP_004027.2:p.Ala927Val