Canonical Allele Identifier: CA346062840

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046160T>A (hg19) ; chr2:g.24823291T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823291T>A , CM000664.2:g.24823291T>A	GRCh38
NC_000002.11:g.25046160T>A , CM000664.1:g.25046160T>A	GRCh37
NC_000002.10:g.24899664T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2804A>T	ENSP00000384484.2:p.Asp935Val
ENST00000679454.1:c.2801A>T MANE Select	ENSP00000505261.1:p.Asp934Val
ENST00000260600.9:c.2801A>T	ENSP00000260600.5:p.Asp934Val
ENST00000405392.5:c.2804A>T	ENSP00000384484.2:p.Asp935Val
ENST00000485887.1:n.73A>T
ENST00000606682.5:c.1742A>T	ENSP00000475652.1:p.Asp581Val
NM_004036.3:c.2801A>T	NP_004027.2:p.Asp934Val
XM_005264104.1:c.2804A>T	XP_005264161.1:p.Asp935Val
XM_005264105.1:c.2801A>T	XP_005264162.1:p.Asp934Val
XM_006711925.1:c.2870A>T	XP_006711988.1:p.Asp957Val
XM_011532489.1:c.2927A>T	XP_011530791.1:p.Asp976Val
XM_011532490.1:c.2924A>T	XP_011530792.1:p.Asp975Val
XM_011532491.1:c.2861A>T	XP_011530793.1:p.Asp954Val
XM_011532492.1:c.2927A>T	XP_011530794.1:p.Asp976Val
XM_011532493.1:c.2789A>T	XP_011530795.1:p.Asp930Val
XM_011532494.1:c.2729A>T	XP_011530796.1:p.Asp910Val
XM_011532495.1:c.2261A>T	XP_011530797.1:p.Asp754Val
XM_011532496.1:c.2204A>T	XP_011530798.1:p.Asp735Val
NM_001320613.1:c.2804A>T	NP_001307542.1:p.Asp935Val
NM_004036.4:c.2801A>T	NP_004027.2:p.Asp934Val
XM_011532492.2:c.2927A>T	XP_011530794.1:p.Asp976Val
XM_017003186.1:c.2867A>T	XP_016858675.1:p.Asp956Val
XM_017003187.1:c.2858A>T	XP_016858676.1:p.Asp953Val
XM_017003188.1:c.2924A>T	XP_016858677.1:p.Asp975Val
XM_017003189.1:c.2786A>T	XP_016858678.1:p.Asp929Val
XM_017003190.1:c.2663A>T	XP_016858679.1:p.Asp888Val
XM_017003191.1:c.2291A>T	XP_016858680.1:p.Asp764Val
XM_017003192.1:c.2081A>T	XP_016858681.1:p.Asp694Val
XM_017003193.1:c.2078A>T	XP_016858682.1:p.Asp693Val
NM_001320613.2:c.2804A>T	NP_001307542.1:p.Asp935Val
NM_001377128.1:c.2867A>T	NP_001364057.1:p.Asp956Val
NM_001377129.1:c.2663A>T	NP_001364058.1:p.Asp888Val
NM_001377130.1:c.2332-661A>T	NP_001364059.1:n.2332-661A>T
NM_001377131.1:c.2078A>T	NP_001364060.1:p.Asp693Val
NM_001377132.1:c.2801A>T	NP_001364061.1:p.Asp934Val
NM_004036.5:c.2801A>T MANE Select	NP_004027.2:p.Asp934Val