Canonical Allele Identifier: CA346062886

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046169T>A (hg19) ; chr2:g.24823300T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823300T>A , CM000664.2:g.24823300T>A	GRCh38
NC_000002.11:g.25046169T>A , CM000664.1:g.25046169T>A	GRCh37
NC_000002.10:g.24899673T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2795A>T	ENSP00000384484.2:p.Asn932Ile
ENST00000679454.1:c.2792A>T MANE Select	ENSP00000505261.1:p.Asn931Ile
ENST00000260600.9:c.2792A>T	ENSP00000260600.5:p.Asn931Ile
ENST00000405392.5:c.2795A>T	ENSP00000384484.2:p.Asn932Ile
ENST00000485887.1:n.64A>T
ENST00000606682.5:c.1733A>T	ENSP00000475652.1:p.Asn578Ile
NM_004036.3:c.2792A>T	NP_004027.2:p.Asn931Ile
XM_005264104.1:c.2795A>T	XP_005264161.1:p.Asn932Ile
XM_005264105.1:c.2792A>T	XP_005264162.1:p.Asn931Ile
XM_006711925.1:c.2861A>T	XP_006711988.1:p.Asn954Ile
XM_011532489.1:c.2918A>T	XP_011530791.1:p.Asn973Ile
XM_011532490.1:c.2915A>T	XP_011530792.1:p.Asn972Ile
XM_011532491.1:c.2852A>T	XP_011530793.1:p.Asn951Ile
XM_011532492.1:c.2918A>T	XP_011530794.1:p.Asn973Ile
XM_011532493.1:c.2780A>T	XP_011530795.1:p.Asn927Ile
XM_011532494.1:c.2720A>T	XP_011530796.1:p.Asn907Ile
XM_011532495.1:c.2252A>T	XP_011530797.1:p.Asn751Ile
XM_011532496.1:c.2195A>T	XP_011530798.1:p.Asn732Ile
NM_001320613.1:c.2795A>T	NP_001307542.1:p.Asn932Ile
NM_004036.4:c.2792A>T	NP_004027.2:p.Asn931Ile
XM_011532492.2:c.2918A>T	XP_011530794.1:p.Asn973Ile
XM_017003186.1:c.2858A>T	XP_016858675.1:p.Asn953Ile
XM_017003187.1:c.2849A>T	XP_016858676.1:p.Asn950Ile
XM_017003188.1:c.2915A>T	XP_016858677.1:p.Asn972Ile
XM_017003189.1:c.2777A>T	XP_016858678.1:p.Asn926Ile
XM_017003190.1:c.2654A>T	XP_016858679.1:p.Asn885Ile
XM_017003191.1:c.2282A>T	XP_016858680.1:p.Asn761Ile
XM_017003192.1:c.2072A>T	XP_016858681.1:p.Asn691Ile
XM_017003193.1:c.2069A>T	XP_016858682.1:p.Asn690Ile
NM_001320613.2:c.2795A>T	NP_001307542.1:p.Asn932Ile
NM_001377128.1:c.2858A>T	NP_001364057.1:p.Asn953Ile
NM_001377129.1:c.2654A>T	NP_001364058.1:p.Asn885Ile
NM_001377130.1:c.2332-670A>T	NP_001364059.1:n.2332-670A>T
NM_001377131.1:c.2069A>T	NP_001364060.1:p.Asn690Ile
NM_001377132.1:c.2792A>T	NP_001364061.1:p.Asn931Ile
NM_004036.5:c.2792A>T MANE Select	NP_004027.2:p.Asn931Ile