Canonical Allele Identifier: CA346063080

Gene: ADCY3

Linked Data

• dbSNP Id: rs1256044558
• MyVariant Identifiers: chr2:g.25046212G>A (hg19) ; chr2:g.24823343G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2752C>T	ENSP00000384484.2:p.Gln918Ter
ENST00000679454.1:c.2749C>T MANE Select	ENSP00000505261.1:p.Gln917Ter
ENST00000260600.9:c.2749C>T	ENSP00000260600.5:p.Gln917Ter
ENST00000405392.5:c.2752C>T	ENSP00000384484.2:p.Gln918Ter
ENST00000485887.1:n.21C>T
ENST00000606682.5:c.1690C>T	ENSP00000475652.1:p.Gln564Ter
NM_004036.3:c.2749C>T	NP_004027.2:p.Gln917Ter
XM_005264104.1:c.2752C>T	XP_005264161.1:p.Gln918Ter
XM_005264105.1:c.2749C>T	XP_005264162.1:p.Gln917Ter
XM_006711925.1:c.2818C>T	XP_006711988.1:p.Gln940Ter
XM_011532489.1:c.2875C>T	XP_011530791.1:p.Gln959Ter
XM_011532490.1:c.2872C>T	XP_011530792.1:p.Gln958Ter
XM_011532491.1:c.2809C>T	XP_011530793.1:p.Gln937Ter
XM_011532492.1:c.2875C>T	XP_011530794.1:p.Gln959Ter
XM_011532493.1:c.2737C>T	XP_011530795.1:p.Gln913Ter
XM_011532494.1:c.2677C>T	XP_011530796.1:p.Gln893Ter
XM_011532495.1:c.2209C>T	XP_011530797.1:p.Gln737Ter
XM_011532496.1:c.2152C>T	XP_011530798.1:p.Gln718Ter
NM_001320613.1:c.2752C>T	NP_001307542.1:p.Gln918Ter
NM_004036.4:c.2749C>T	NP_004027.2:p.Gln917Ter
XM_011532492.2:c.2875C>T	XP_011530794.1:p.Gln959Ter
XM_017003186.1:c.2815C>T	XP_016858675.1:p.Gln939Ter
XM_017003187.1:c.2806C>T	XP_016858676.1:p.Gln936Ter
XM_017003188.1:c.2872C>T	XP_016858677.1:p.Gln958Ter
XM_017003189.1:c.2734C>T	XP_016858678.1:p.Gln912Ter
XM_017003190.1:c.2611C>T	XP_016858679.1:p.Gln871Ter
XM_017003191.1:c.2239C>T	XP_016858680.1:p.Gln747Ter
XM_017003192.1:c.2029C>T	XP_016858681.1:p.Gln677Ter
XM_017003193.1:c.2026C>T	XP_016858682.1:p.Gln676Ter
NM_001320613.2:c.2752C>T	NP_001307542.1:p.Gln918Ter
NM_001377128.1:c.2815C>T	NP_001364057.1:p.Gln939Ter
NM_001377129.1:c.2611C>T	NP_001364058.1:p.Gln871Ter
NM_001377130.1:c.2332-713C>T	NP_001364059.1:n.2332-713C>T
NM_001377131.1:c.2026C>T	NP_001364060.1:p.Gln676Ter
NM_001377132.1:c.2749C>T	NP_001364061.1:p.Gln917Ter
NM_004036.5:c.2749C>T MANE Select	NP_004027.2:p.Gln917Ter