Canonical Allele Identifier: CA1553610

Gene: ADCY3

Linked Data

• ClinVar Variation Id: 3043752
• ClinVar RCV Id: RCV003936956
• dbSNP Id: rs375101795
• ExAC: 2:25046159 G / A
• gnomAD v2: 2-25046159-G-A
• gnomAD v3: 2-24823290-G-A
• gnomAD v4: 2-24823290-G-A
• MyVariant Identifiers: chr2:g.25046159G>A (hg19) ; chr2:g.24823290G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823290G>A , CM000664.2:g.24823290G>A	GRCh38
NC_000002.11:g.25046159G>A , CM000664.1:g.25046159G>A	GRCh37
NC_000002.10:g.24899663G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2805C>T	ENSP00000384484.2:p.Asp935=
ENST00000679454.1:c.2802C>T MANE Select	ENSP00000505261.1:p.Asp934=
ENST00000260600.9:c.2802C>T	ENSP00000260600.5:p.Asp934=
ENST00000405392.5:c.2805C>T	ENSP00000384484.2:p.Asp935=
ENST00000485887.1:n.74C>T
ENST00000606682.5:c.1743C>T	ENSP00000475652.1:p.Asp581=
NM_004036.3:c.2802C>T	NP_004027.2:p.Asp934=
XM_005264104.1:c.2805C>T	XP_005264161.1:p.Asp935=
XM_005264105.1:c.2802C>T	XP_005264162.1:p.Asp934=
XM_006711925.1:c.2871C>T	XP_006711988.1:p.Asp957=
XM_011532489.1:c.2928C>T	XP_011530791.1:p.Asp976=
XM_011532490.1:c.2925C>T	XP_011530792.1:p.Asp975=
XM_011532491.1:c.2862C>T	XP_011530793.1:p.Asp954=
XM_011532492.1:c.2928C>T	XP_011530794.1:p.Asp976=
XM_011532493.1:c.2790C>T	XP_011530795.1:p.Asp930=
XM_011532494.1:c.2730C>T	XP_011530796.1:p.Asp910=
XM_011532495.1:c.2262C>T	XP_011530797.1:p.Asp754=
XM_011532496.1:c.2205C>T	XP_011530798.1:p.Asp735=
NM_001320613.1:c.2805C>T	NP_001307542.1:p.Asp935=
NM_004036.4:c.2802C>T	NP_004027.2:p.Asp934=
XM_011532492.2:c.2928C>T	XP_011530794.1:p.Asp976=
XM_017003186.1:c.2868C>T	XP_016858675.1:p.Asp956=
XM_017003187.1:c.2859C>T	XP_016858676.1:p.Asp953=
XM_017003188.1:c.2925C>T	XP_016858677.1:p.Asp975=
XM_017003189.1:c.2787C>T	XP_016858678.1:p.Asp929=
XM_017003190.1:c.2664C>T	XP_016858679.1:p.Asp888=
XM_017003191.1:c.2292C>T	XP_016858680.1:p.Asp764=
XM_017003192.1:c.2082C>T	XP_016858681.1:p.Asp694=
XM_017003193.1:c.2079C>T	XP_016858682.1:p.Asp693=
NM_001320613.2:c.2805C>T	NP_001307542.1:p.Asp935=
NM_001377128.1:c.2868C>T	NP_001364057.1:p.Asp956=
NM_001377129.1:c.2664C>T	NP_001364058.1:p.Asp888=
NM_001377130.1:c.2332-660C>T	NP_001364059.1:n.2332-660C>T
NM_001377131.1:c.2079C>T	NP_001364060.1:p.Asp693=
NM_001377132.1:c.2802C>T	NP_001364061.1:p.Asp934=
NM_004036.5:c.2802C>T MANE Select	NP_004027.2:p.Asp934=