Canonical Allele Identifier: CA346062889

Gene: ADCY3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2795A>C	ENSP00000384484.2:p.Asn932Thr
ENST00000679454.1:c.2792A>C MANE Select	ENSP00000505261.1:p.Asn931Thr
ENST00000260600.9:c.2792A>C	ENSP00000260600.5:p.Asn931Thr
ENST00000405392.5:c.2795A>C	ENSP00000384484.2:p.Asn932Thr
ENST00000485887.1:n.64A>C
ENST00000606682.5:c.1733A>C	ENSP00000475652.1:p.Asn578Thr
NM_004036.3:c.2792A>C	NP_004027.2:p.Asn931Thr
XM_005264104.1:c.2795A>C	XP_005264161.1:p.Asn932Thr
XM_005264105.1:c.2792A>C	XP_005264162.1:p.Asn931Thr
XM_006711925.1:c.2861A>C	XP_006711988.1:p.Asn954Thr
XM_011532489.1:c.2918A>C	XP_011530791.1:p.Asn973Thr
XM_011532490.1:c.2915A>C	XP_011530792.1:p.Asn972Thr
XM_011532491.1:c.2852A>C	XP_011530793.1:p.Asn951Thr
XM_011532492.1:c.2918A>C	XP_011530794.1:p.Asn973Thr
XM_011532493.1:c.2780A>C	XP_011530795.1:p.Asn927Thr
XM_011532494.1:c.2720A>C	XP_011530796.1:p.Asn907Thr
XM_011532495.1:c.2252A>C	XP_011530797.1:p.Asn751Thr
XM_011532496.1:c.2195A>C	XP_011530798.1:p.Asn732Thr
NM_001320613.1:c.2795A>C	NP_001307542.1:p.Asn932Thr
NM_004036.4:c.2792A>C	NP_004027.2:p.Asn931Thr
XM_011532492.2:c.2918A>C	XP_011530794.1:p.Asn973Thr
XM_017003186.1:c.2858A>C	XP_016858675.1:p.Asn953Thr
XM_017003187.1:c.2849A>C	XP_016858676.1:p.Asn950Thr
XM_017003188.1:c.2915A>C	XP_016858677.1:p.Asn972Thr
XM_017003189.1:c.2777A>C	XP_016858678.1:p.Asn926Thr
XM_017003190.1:c.2654A>C	XP_016858679.1:p.Asn885Thr
XM_017003191.1:c.2282A>C	XP_016858680.1:p.Asn761Thr
XM_017003192.1:c.2072A>C	XP_016858681.1:p.Asn691Thr
XM_017003193.1:c.2069A>C	XP_016858682.1:p.Asn690Thr
NM_001320613.2:c.2795A>C	NP_001307542.1:p.Asn932Thr
NM_001377128.1:c.2858A>C	NP_001364057.1:p.Asn953Thr
NM_001377129.1:c.2654A>C	NP_001364058.1:p.Asn885Thr
NM_001377130.1:c.2332-670A>C	NP_001364059.1:n.2332-670A>C
NM_001377131.1:c.2069A>C	NP_001364060.1:p.Asn690Thr
NM_001377132.1:c.2792A>C	NP_001364061.1:p.Asn931Thr
NM_004036.5:c.2792A>C MANE Select	NP_004027.2:p.Asn931Thr