Canonical Allele Identifier: CA346062971

Gene: ADCY3

Linked Data

• dbSNP Id: rs1668058328
• gnomAD v4: 2-24823319-T-C
• MyVariant Identifiers: chr2:g.25046188T>C (hg19) ; chr2:g.24823319T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823319T>C , CM000664.2:g.24823319T>C	GRCh38
NC_000002.11:g.25046188T>C , CM000664.1:g.25046188T>C	GRCh37
NC_000002.10:g.24899692T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2776A>G	ENSP00000384484.2:p.Met926Val
ENST00000679454.1:c.2773A>G MANE Select	ENSP00000505261.1:p.Met925Val
ENST00000260600.9:c.2773A>G	ENSP00000260600.5:p.Met925Val
ENST00000405392.5:c.2776A>G	ENSP00000384484.2:p.Met926Val
ENST00000485887.1:n.45A>G
ENST00000606682.5:c.1714A>G	ENSP00000475652.1:p.Met572Val
NM_004036.3:c.2773A>G	NP_004027.2:p.Met925Val
XM_005264104.1:c.2776A>G	XP_005264161.1:p.Met926Val
XM_005264105.1:c.2773A>G	XP_005264162.1:p.Met925Val
XM_006711925.1:c.2842A>G	XP_006711988.1:p.Met948Val
XM_011532489.1:c.2899A>G	XP_011530791.1:p.Met967Val
XM_011532490.1:c.2896A>G	XP_011530792.1:p.Met966Val
XM_011532491.1:c.2833A>G	XP_011530793.1:p.Met945Val
XM_011532492.1:c.2899A>G	XP_011530794.1:p.Met967Val
XM_011532493.1:c.2761A>G	XP_011530795.1:p.Met921Val
XM_011532494.1:c.2701A>G	XP_011530796.1:p.Met901Val
XM_011532495.1:c.2233A>G	XP_011530797.1:p.Met745Val
XM_011532496.1:c.2176A>G	XP_011530798.1:p.Met726Val
NM_001320613.1:c.2776A>G	NP_001307542.1:p.Met926Val
NM_004036.4:c.2773A>G	NP_004027.2:p.Met925Val
XM_011532492.2:c.2899A>G	XP_011530794.1:p.Met967Val
XM_017003186.1:c.2839A>G	XP_016858675.1:p.Met947Val
XM_017003187.1:c.2830A>G	XP_016858676.1:p.Met944Val
XM_017003188.1:c.2896A>G	XP_016858677.1:p.Met966Val
XM_017003189.1:c.2758A>G	XP_016858678.1:p.Met920Val
XM_017003190.1:c.2635A>G	XP_016858679.1:p.Met879Val
XM_017003191.1:c.2263A>G	XP_016858680.1:p.Met755Val
XM_017003192.1:c.2053A>G	XP_016858681.1:p.Met685Val
XM_017003193.1:c.2050A>G	XP_016858682.1:p.Met684Val
NM_001320613.2:c.2776A>G	NP_001307542.1:p.Met926Val
NM_001377128.1:c.2839A>G	NP_001364057.1:p.Met947Val
NM_001377129.1:c.2635A>G	NP_001364058.1:p.Met879Val
NM_001377130.1:c.2332-689A>G	NP_001364059.1:n.2332-689A>G
NM_001377131.1:c.2050A>G	NP_001364060.1:p.Met684Val
NM_001377132.1:c.2773A>G	NP_001364061.1:p.Met925Val
NM_004036.5:c.2773A>G MANE Select	NP_004027.2:p.Met925Val