Canonical Allele Identifier: CA346063082

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046212G>C (hg19) ; chr2:g.24823343G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823343G>C , CM000664.2:g.24823343G>C	GRCh38
NC_000002.11:g.25046212G>C , CM000664.1:g.25046212G>C	GRCh37
NC_000002.10:g.24899716G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2752C>G	ENSP00000384484.2:p.Gln918Glu
ENST00000679454.1:c.2749C>G MANE Select	ENSP00000505261.1:p.Gln917Glu
ENST00000260600.9:c.2749C>G	ENSP00000260600.5:p.Gln917Glu
ENST00000405392.5:c.2752C>G	ENSP00000384484.2:p.Gln918Glu
ENST00000485887.1:n.21C>G
ENST00000606682.5:c.1690C>G	ENSP00000475652.1:p.Gln564Glu
NM_004036.3:c.2749C>G	NP_004027.2:p.Gln917Glu
XM_005264104.1:c.2752C>G	XP_005264161.1:p.Gln918Glu
XM_005264105.1:c.2749C>G	XP_005264162.1:p.Gln917Glu
XM_006711925.1:c.2818C>G	XP_006711988.1:p.Gln940Glu
XM_011532489.1:c.2875C>G	XP_011530791.1:p.Gln959Glu
XM_011532490.1:c.2872C>G	XP_011530792.1:p.Gln958Glu
XM_011532491.1:c.2809C>G	XP_011530793.1:p.Gln937Glu
XM_011532492.1:c.2875C>G	XP_011530794.1:p.Gln959Glu
XM_011532493.1:c.2737C>G	XP_011530795.1:p.Gln913Glu
XM_011532494.1:c.2677C>G	XP_011530796.1:p.Gln893Glu
XM_011532495.1:c.2209C>G	XP_011530797.1:p.Gln737Glu
XM_011532496.1:c.2152C>G	XP_011530798.1:p.Gln718Glu
NM_001320613.1:c.2752C>G	NP_001307542.1:p.Gln918Glu
NM_004036.4:c.2749C>G	NP_004027.2:p.Gln917Glu
XM_011532492.2:c.2875C>G	XP_011530794.1:p.Gln959Glu
XM_017003186.1:c.2815C>G	XP_016858675.1:p.Gln939Glu
XM_017003187.1:c.2806C>G	XP_016858676.1:p.Gln936Glu
XM_017003188.1:c.2872C>G	XP_016858677.1:p.Gln958Glu
XM_017003189.1:c.2734C>G	XP_016858678.1:p.Gln912Glu
XM_017003190.1:c.2611C>G	XP_016858679.1:p.Gln871Glu
XM_017003191.1:c.2239C>G	XP_016858680.1:p.Gln747Glu
XM_017003192.1:c.2029C>G	XP_016858681.1:p.Gln677Glu
XM_017003193.1:c.2026C>G	XP_016858682.1:p.Gln676Glu
NM_001320613.2:c.2752C>G	NP_001307542.1:p.Gln918Glu
NM_001377128.1:c.2815C>G	NP_001364057.1:p.Gln939Glu
NM_001377129.1:c.2611C>G	NP_001364058.1:p.Gln871Glu
NM_001377130.1:c.2332-713C>G	NP_001364059.1:n.2332-713C>G
NM_001377131.1:c.2026C>G	NP_001364060.1:p.Gln676Glu
NM_001377132.1:c.2749C>G	NP_001364061.1:p.Gln917Glu
NM_004036.5:c.2749C>G MANE Select	NP_004027.2:p.Gln917Glu