Canonical Allele Identifier: CA346062893

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046170T>C (hg19) ; chr2:g.24823301T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823301T>C , CM000664.2:g.24823301T>C	GRCh38
NC_000002.11:g.25046170T>C , CM000664.1:g.25046170T>C	GRCh37
NC_000002.10:g.24899674T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2794A>G	ENSP00000384484.2:p.Asn932Asp
ENST00000679454.1:c.2791A>G MANE Select	ENSP00000505261.1:p.Asn931Asp
ENST00000260600.9:c.2791A>G	ENSP00000260600.5:p.Asn931Asp
ENST00000405392.5:c.2794A>G	ENSP00000384484.2:p.Asn932Asp
ENST00000485887.1:n.63A>G
ENST00000606682.5:c.1732A>G	ENSP00000475652.1:p.Asn578Asp
NM_004036.3:c.2791A>G	NP_004027.2:p.Asn931Asp
XM_005264104.1:c.2794A>G	XP_005264161.1:p.Asn932Asp
XM_005264105.1:c.2791A>G	XP_005264162.1:p.Asn931Asp
XM_006711925.1:c.2860A>G	XP_006711988.1:p.Asn954Asp
XM_011532489.1:c.2917A>G	XP_011530791.1:p.Asn973Asp
XM_011532490.1:c.2914A>G	XP_011530792.1:p.Asn972Asp
XM_011532491.1:c.2851A>G	XP_011530793.1:p.Asn951Asp
XM_011532492.1:c.2917A>G	XP_011530794.1:p.Asn973Asp
XM_011532493.1:c.2779A>G	XP_011530795.1:p.Asn927Asp
XM_011532494.1:c.2719A>G	XP_011530796.1:p.Asn907Asp
XM_011532495.1:c.2251A>G	XP_011530797.1:p.Asn751Asp
XM_011532496.1:c.2194A>G	XP_011530798.1:p.Asn732Asp
NM_001320613.1:c.2794A>G	NP_001307542.1:p.Asn932Asp
NM_004036.4:c.2791A>G	NP_004027.2:p.Asn931Asp
XM_011532492.2:c.2917A>G	XP_011530794.1:p.Asn973Asp
XM_017003186.1:c.2857A>G	XP_016858675.1:p.Asn953Asp
XM_017003187.1:c.2848A>G	XP_016858676.1:p.Asn950Asp
XM_017003188.1:c.2914A>G	XP_016858677.1:p.Asn972Asp
XM_017003189.1:c.2776A>G	XP_016858678.1:p.Asn926Asp
XM_017003190.1:c.2653A>G	XP_016858679.1:p.Asn885Asp
XM_017003191.1:c.2281A>G	XP_016858680.1:p.Asn761Asp
XM_017003192.1:c.2071A>G	XP_016858681.1:p.Asn691Asp
XM_017003193.1:c.2068A>G	XP_016858682.1:p.Asn690Asp
NM_001320613.2:c.2794A>G	NP_001307542.1:p.Asn932Asp
NM_001377128.1:c.2857A>G	NP_001364057.1:p.Asn953Asp
NM_001377129.1:c.2653A>G	NP_001364058.1:p.Asn885Asp
NM_001377130.1:c.2332-671A>G	NP_001364059.1:n.2332-671A>G
NM_001377131.1:c.2068A>G	NP_001364060.1:p.Asn690Asp
NM_001377132.1:c.2791A>G	NP_001364061.1:p.Asn931Asp
NM_004036.5:c.2791A>G MANE Select	NP_004027.2:p.Asn931Asp