Canonical Allele Identifier: CA346062913

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046175A>C (hg19) ; chr2:g.24823306A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823306A>C , CM000664.2:g.24823306A>C	GRCh38
NC_000002.11:g.25046175A>C , CM000664.1:g.25046175A>C	GRCh37
NC_000002.10:g.24899679A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2789T>G	ENSP00000384484.2:p.Leu930Arg
ENST00000679454.1:c.2786T>G MANE Select	ENSP00000505261.1:p.Leu929Arg
ENST00000260600.9:c.2786T>G	ENSP00000260600.5:p.Leu929Arg
ENST00000405392.5:c.2789T>G	ENSP00000384484.2:p.Leu930Arg
ENST00000485887.1:n.58T>G
ENST00000606682.5:c.1727T>G	ENSP00000475652.1:p.Leu576Arg
NM_004036.3:c.2786T>G	NP_004027.2:p.Leu929Arg
XM_005264104.1:c.2789T>G	XP_005264161.1:p.Leu930Arg
XM_005264105.1:c.2786T>G	XP_005264162.1:p.Leu929Arg
XM_006711925.1:c.2855T>G	XP_006711988.1:p.Leu952Arg
XM_011532489.1:c.2912T>G	XP_011530791.1:p.Leu971Arg
XM_011532490.1:c.2909T>G	XP_011530792.1:p.Leu970Arg
XM_011532491.1:c.2846T>G	XP_011530793.1:p.Leu949Arg
XM_011532492.1:c.2912T>G	XP_011530794.1:p.Leu971Arg
XM_011532493.1:c.2774T>G	XP_011530795.1:p.Leu925Arg
XM_011532494.1:c.2714T>G	XP_011530796.1:p.Leu905Arg
XM_011532495.1:c.2246T>G	XP_011530797.1:p.Leu749Arg
XM_011532496.1:c.2189T>G	XP_011530798.1:p.Leu730Arg
NM_001320613.1:c.2789T>G	NP_001307542.1:p.Leu930Arg
NM_004036.4:c.2786T>G	NP_004027.2:p.Leu929Arg
XM_011532492.2:c.2912T>G	XP_011530794.1:p.Leu971Arg
XM_017003186.1:c.2852T>G	XP_016858675.1:p.Leu951Arg
XM_017003187.1:c.2843T>G	XP_016858676.1:p.Leu948Arg
XM_017003188.1:c.2909T>G	XP_016858677.1:p.Leu970Arg
XM_017003189.1:c.2771T>G	XP_016858678.1:p.Leu924Arg
XM_017003190.1:c.2648T>G	XP_016858679.1:p.Leu883Arg
XM_017003191.1:c.2276T>G	XP_016858680.1:p.Leu759Arg
XM_017003192.1:c.2066T>G	XP_016858681.1:p.Leu689Arg
XM_017003193.1:c.2063T>G	XP_016858682.1:p.Leu688Arg
NM_001320613.2:c.2789T>G	NP_001307542.1:p.Leu930Arg
NM_001377128.1:c.2852T>G	NP_001364057.1:p.Leu951Arg
NM_001377129.1:c.2648T>G	NP_001364058.1:p.Leu883Arg
NM_001377130.1:c.2332-676T>G	NP_001364059.1:n.2332-676T>G
NM_001377131.1:c.2063T>G	NP_001364060.1:p.Leu688Arg
NM_001377132.1:c.2786T>G	NP_001364061.1:p.Leu929Arg
NM_004036.5:c.2786T>G MANE Select	NP_004027.2:p.Leu929Arg