Canonical Allele Identifier: CA346062931

Gene: ADCY3

Linked Data

• gnomAD v4: 2-24823310-A-C
• MyVariant Identifiers: chr2:g.25046179A>C (hg19) ; chr2:g.24823310A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823310A>C , CM000664.2:g.24823310A>C	GRCh38
NC_000002.11:g.25046179A>C , CM000664.1:g.25046179A>C	GRCh37
NC_000002.10:g.24899683A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2785T>G	ENSP00000384484.2:p.Ser929Ala
ENST00000679454.1:c.2782T>G MANE Select	ENSP00000505261.1:p.Ser928Ala
ENST00000260600.9:c.2782T>G	ENSP00000260600.5:p.Ser928Ala
ENST00000405392.5:c.2785T>G	ENSP00000384484.2:p.Ser929Ala
ENST00000485887.1:n.54T>G
ENST00000606682.5:c.1723T>G	ENSP00000475652.1:p.Ser575Ala
NM_004036.3:c.2782T>G	NP_004027.2:p.Ser928Ala
XM_005264104.1:c.2785T>G	XP_005264161.1:p.Ser929Ala
XM_005264105.1:c.2782T>G	XP_005264162.1:p.Ser928Ala
XM_006711925.1:c.2851T>G	XP_006711988.1:p.Ser951Ala
XM_011532489.1:c.2908T>G	XP_011530791.1:p.Ser970Ala
XM_011532490.1:c.2905T>G	XP_011530792.1:p.Ser969Ala
XM_011532491.1:c.2842T>G	XP_011530793.1:p.Ser948Ala
XM_011532492.1:c.2908T>G	XP_011530794.1:p.Ser970Ala
XM_011532493.1:c.2770T>G	XP_011530795.1:p.Ser924Ala
XM_011532494.1:c.2710T>G	XP_011530796.1:p.Ser904Ala
XM_011532495.1:c.2242T>G	XP_011530797.1:p.Ser748Ala
XM_011532496.1:c.2185T>G	XP_011530798.1:p.Ser729Ala
NM_001320613.1:c.2785T>G	NP_001307542.1:p.Ser929Ala
NM_004036.4:c.2782T>G	NP_004027.2:p.Ser928Ala
XM_011532492.2:c.2908T>G	XP_011530794.1:p.Ser970Ala
XM_017003186.1:c.2848T>G	XP_016858675.1:p.Ser950Ala
XM_017003187.1:c.2839T>G	XP_016858676.1:p.Ser947Ala
XM_017003188.1:c.2905T>G	XP_016858677.1:p.Ser969Ala
XM_017003189.1:c.2767T>G	XP_016858678.1:p.Ser923Ala
XM_017003190.1:c.2644T>G	XP_016858679.1:p.Ser882Ala
XM_017003191.1:c.2272T>G	XP_016858680.1:p.Ser758Ala
XM_017003192.1:c.2062T>G	XP_016858681.1:p.Ser688Ala
XM_017003193.1:c.2059T>G	XP_016858682.1:p.Ser687Ala
NM_001320613.2:c.2785T>G	NP_001307542.1:p.Ser929Ala
NM_001377128.1:c.2848T>G	NP_001364057.1:p.Ser950Ala
NM_001377129.1:c.2644T>G	NP_001364058.1:p.Ser882Ala
NM_001377130.1:c.2332-680T>G	NP_001364059.1:n.2332-680T>G
NM_001377131.1:c.2059T>G	NP_001364060.1:p.Ser687Ala
NM_001377132.1:c.2782T>G	NP_001364061.1:p.Ser928Ala
NM_004036.5:c.2782T>G MANE Select	NP_004027.2:p.Ser928Ala