Canonical Allele Identifier: CA346062496

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046092A>C (hg19) ; chr2:g.24823223A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823223A>C , CM000664.2:g.24823223A>C	GRCh38
NC_000002.11:g.25046092A>C , CM000664.1:g.25046092A>C	GRCh37
NC_000002.10:g.24899596A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2872T>G	ENSP00000384484.2:p.Ser958Ala
ENST00000679454.1:c.2869T>G MANE Select	ENSP00000505261.1:p.Ser957Ala
ENST00000260600.9:c.2869T>G	ENSP00000260600.5:p.Ser957Ala
ENST00000405392.5:c.2872T>G	ENSP00000384484.2:p.Ser958Ala
ENST00000485887.1:n.141T>G
ENST00000606682.5:c.1810T>G	ENSP00000475652.1:p.Ser604Ala
NM_004036.3:c.2869T>G	NP_004027.2:p.Ser957Ala
XM_005264104.1:c.2872T>G	XP_005264161.1:p.Ser958Ala
XM_005264105.1:c.2869T>G	XP_005264162.1:p.Ser957Ala
XM_006711925.1:c.2938T>G	XP_006711988.1:p.Ser980Ala
XM_011532489.1:c.2995T>G	XP_011530791.1:p.Ser999Ala
XM_011532490.1:c.2992T>G	XP_011530792.1:p.Ser998Ala
XM_011532491.1:c.2929T>G	XP_011530793.1:p.Ser977Ala
XM_011532492.1:c.2995T>G	XP_011530794.1:p.Ser999Ala
XM_011532493.1:c.2857T>G	XP_011530795.1:p.Ser953Ala
XM_011532494.1:c.2797T>G	XP_011530796.1:p.Ser933Ala
XM_011532495.1:c.2329T>G	XP_011530797.1:p.Ser777Ala
XM_011532496.1:c.2272T>G	XP_011530798.1:p.Ser758Ala
NM_001320613.1:c.2872T>G	NP_001307542.1:p.Ser958Ala
NM_004036.4:c.2869T>G	NP_004027.2:p.Ser957Ala
XM_011532492.2:c.2995T>G	XP_011530794.1:p.Ser999Ala
XM_017003186.1:c.2935T>G	XP_016858675.1:p.Ser979Ala
XM_017003187.1:c.2926T>G	XP_016858676.1:p.Ser976Ala
XM_017003188.1:c.2992T>G	XP_016858677.1:p.Ser998Ala
XM_017003189.1:c.2854T>G	XP_016858678.1:p.Ser952Ala
XM_017003190.1:c.2731T>G	XP_016858679.1:p.Ser911Ala
XM_017003191.1:c.2359T>G	XP_016858680.1:p.Ser787Ala
XM_017003192.1:c.2149T>G	XP_016858681.1:p.Ser717Ala
XM_017003193.1:c.2146T>G	XP_016858682.1:p.Ser716Ala
NM_001320613.2:c.2872T>G	NP_001307542.1:p.Ser958Ala
NM_001377128.1:c.2935T>G	NP_001364057.1:p.Ser979Ala
NM_001377129.1:c.2731T>G	NP_001364058.1:p.Ser911Ala
NM_001377130.1:c.2332-593T>G	NP_001364059.1:n.2332-593T>G
NM_001377131.1:c.2146T>G	NP_001364060.1:p.Ser716Ala
NM_001377132.1:c.2869T>G	NP_001364061.1:p.Ser957Ala
NM_004036.5:c.2869T>G MANE Select	NP_004027.2:p.Ser957Ala