Canonical Allele Identifier: CA346062844

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046161C>A (hg19) ; chr2:g.24823292C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823292C>A , CM000664.2:g.24823292C>A	GRCh38
NC_000002.11:g.25046161C>A , CM000664.1:g.25046161C>A	GRCh37
NC_000002.10:g.24899665C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2803G>T	ENSP00000384484.2:p.Asp935Tyr
ENST00000679454.1:c.2800G>T MANE Select	ENSP00000505261.1:p.Asp934Tyr
ENST00000260600.9:c.2800G>T	ENSP00000260600.5:p.Asp934Tyr
ENST00000405392.5:c.2803G>T	ENSP00000384484.2:p.Asp935Tyr
ENST00000485887.1:n.72G>T
ENST00000606682.5:c.1741G>T	ENSP00000475652.1:p.Asp581Tyr
NM_004036.3:c.2800G>T	NP_004027.2:p.Asp934Tyr
XM_005264104.1:c.2803G>T	XP_005264161.1:p.Asp935Tyr
XM_005264105.1:c.2800G>T	XP_005264162.1:p.Asp934Tyr
XM_006711925.1:c.2869G>T	XP_006711988.1:p.Asp957Tyr
XM_011532489.1:c.2926G>T	XP_011530791.1:p.Asp976Tyr
XM_011532490.1:c.2923G>T	XP_011530792.1:p.Asp975Tyr
XM_011532491.1:c.2860G>T	XP_011530793.1:p.Asp954Tyr
XM_011532492.1:c.2926G>T	XP_011530794.1:p.Asp976Tyr
XM_011532493.1:c.2788G>T	XP_011530795.1:p.Asp930Tyr
XM_011532494.1:c.2728G>T	XP_011530796.1:p.Asp910Tyr
XM_011532495.1:c.2260G>T	XP_011530797.1:p.Asp754Tyr
XM_011532496.1:c.2203G>T	XP_011530798.1:p.Asp735Tyr
NM_001320613.1:c.2803G>T	NP_001307542.1:p.Asp935Tyr
NM_004036.4:c.2800G>T	NP_004027.2:p.Asp934Tyr
XM_011532492.2:c.2926G>T	XP_011530794.1:p.Asp976Tyr
XM_017003186.1:c.2866G>T	XP_016858675.1:p.Asp956Tyr
XM_017003187.1:c.2857G>T	XP_016858676.1:p.Asp953Tyr
XM_017003188.1:c.2923G>T	XP_016858677.1:p.Asp975Tyr
XM_017003189.1:c.2785G>T	XP_016858678.1:p.Asp929Tyr
XM_017003190.1:c.2662G>T	XP_016858679.1:p.Asp888Tyr
XM_017003191.1:c.2290G>T	XP_016858680.1:p.Asp764Tyr
XM_017003192.1:c.2080G>T	XP_016858681.1:p.Asp694Tyr
XM_017003193.1:c.2077G>T	XP_016858682.1:p.Asp693Tyr
NM_001320613.2:c.2803G>T	NP_001307542.1:p.Asp935Tyr
NM_001377128.1:c.2866G>T	NP_001364057.1:p.Asp956Tyr
NM_001377129.1:c.2662G>T	NP_001364058.1:p.Asp888Tyr
NM_001377130.1:c.2332-662G>T	NP_001364059.1:n.2332-662G>T
NM_001377131.1:c.2077G>T	NP_001364060.1:p.Asp693Tyr
NM_001377132.1:c.2800G>T	NP_001364061.1:p.Asp934Tyr
NM_004036.5:c.2800G>T MANE Select	NP_004027.2:p.Asp934Tyr