Canonical Allele Identifier: CA346063494

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047286G>T (hg19) ; chr2:g.24824417G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824417G>T , CM000664.2:g.24824417G>T	GRCh38
NC_000002.11:g.25047286G>T , CM000664.1:g.25047286G>T	GRCh37
NC_000002.10:g.24900790G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2700C>A	ENSP00000384484.2:p.His900Gln
ENST00000679454.1:c.2697C>A MANE Select	ENSP00000505261.1:p.His899Gln
ENST00000260600.9:c.2697C>A	ENSP00000260600.5:p.His899Gln
ENST00000405392.5:c.2700C>A	ENSP00000384484.2:p.His900Gln
ENST00000606682.5:c.1638C>A	ENSP00000475652.1:p.His546Gln
NM_004036.3:c.2697C>A	NP_004027.2:p.His899Gln
XM_005264104.1:c.2700C>A	XP_005264161.1:p.His900Gln
XM_005264105.1:c.2697C>A	XP_005264162.1:p.His899Gln
XM_006711925.1:c.2766C>A	XP_006711988.1:p.His922Gln
XM_011532489.1:c.2823C>A	XP_011530791.1:p.His941Gln
XM_011532490.1:c.2820C>A	XP_011530792.1:p.His940Gln
XM_011532491.1:c.2757C>A	XP_011530793.1:p.His919Gln
XM_011532492.1:c.2823C>A	XP_011530794.1:p.His941Gln
XM_011532493.1:c.2685C>A	XP_011530795.1:p.His895Gln
XM_011532494.1:c.2625C>A	XP_011530796.1:p.His875Gln
XM_011532495.1:c.2157C>A	XP_011530797.1:p.His719Gln
XM_011532496.1:c.2100C>A	XP_011530798.1:p.His700Gln
NM_001320613.1:c.2700C>A	NP_001307542.1:p.His900Gln
NM_004036.4:c.2697C>A	NP_004027.2:p.His899Gln
XM_011532492.2:c.2823C>A	XP_011530794.1:p.His941Gln
XM_017003186.1:c.2763C>A	XP_016858675.1:p.His921Gln
XM_017003187.1:c.2754C>A	XP_016858676.1:p.His918Gln
XM_017003188.1:c.2820C>A	XP_016858677.1:p.His940Gln
XM_017003189.1:c.2682C>A	XP_016858678.1:p.His894Gln
XM_017003190.1:c.2559C>A	XP_016858679.1:p.His853Gln
XM_017003191.1:c.2187C>A	XP_016858680.1:p.His729Gln
XM_017003192.1:c.1977C>A	XP_016858681.1:p.His659Gln
XM_017003193.1:c.1974C>A	XP_016858682.1:p.His658Gln
NM_001320613.2:c.2700C>A	NP_001307542.1:p.His900Gln
NM_001377128.1:c.2763C>A	NP_001364057.1:p.His921Gln
NM_001377129.1:c.2559C>A	NP_001364058.1:p.His853Gln
NM_001377130.1:c.2292C>A	NP_001364059.1:p.His764Gln
NM_001377131.1:c.1974C>A	NP_001364060.1:p.His658Gln
NM_001377132.1:c.2697C>A	NP_001364061.1:p.His899Gln
NM_004036.5:c.2697C>A MANE Select	NP_004027.2:p.His899Gln