Canonical Allele Identifier: CA346062546

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046107G>C (hg19) ; chr2:g.24823238G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823238G>C , CM000664.2:g.24823238G>C	GRCh38
NC_000002.11:g.25046107G>C , CM000664.1:g.25046107G>C	GRCh37
NC_000002.10:g.24899611G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2857C>G	ENSP00000384484.2:p.Leu953Val
ENST00000679454.1:c.2854C>G MANE Select	ENSP00000505261.1:p.Leu952Val
ENST00000260600.9:c.2854C>G	ENSP00000260600.5:p.Leu952Val
ENST00000405392.5:c.2857C>G	ENSP00000384484.2:p.Leu953Val
ENST00000485887.1:n.126C>G
ENST00000606682.5:c.1795C>G	ENSP00000475652.1:p.Leu599Val
NM_004036.3:c.2854C>G	NP_004027.2:p.Leu952Val
XM_005264104.1:c.2857C>G	XP_005264161.1:p.Leu953Val
XM_005264105.1:c.2854C>G	XP_005264162.1:p.Leu952Val
XM_006711925.1:c.2923C>G	XP_006711988.1:p.Leu975Val
XM_011532489.1:c.2980C>G	XP_011530791.1:p.Leu994Val
XM_011532490.1:c.2977C>G	XP_011530792.1:p.Leu993Val
XM_011532491.1:c.2914C>G	XP_011530793.1:p.Leu972Val
XM_011532492.1:c.2980C>G	XP_011530794.1:p.Leu994Val
XM_011532493.1:c.2842C>G	XP_011530795.1:p.Leu948Val
XM_011532494.1:c.2782C>G	XP_011530796.1:p.Leu928Val
XM_011532495.1:c.2314C>G	XP_011530797.1:p.Leu772Val
XM_011532496.1:c.2257C>G	XP_011530798.1:p.Leu753Val
NM_001320613.1:c.2857C>G	NP_001307542.1:p.Leu953Val
NM_004036.4:c.2854C>G	NP_004027.2:p.Leu952Val
XM_011532492.2:c.2980C>G	XP_011530794.1:p.Leu994Val
XM_017003186.1:c.2920C>G	XP_016858675.1:p.Leu974Val
XM_017003187.1:c.2911C>G	XP_016858676.1:p.Leu971Val
XM_017003188.1:c.2977C>G	XP_016858677.1:p.Leu993Val
XM_017003189.1:c.2839C>G	XP_016858678.1:p.Leu947Val
XM_017003190.1:c.2716C>G	XP_016858679.1:p.Leu906Val
XM_017003191.1:c.2344C>G	XP_016858680.1:p.Leu782Val
XM_017003192.1:c.2134C>G	XP_016858681.1:p.Leu712Val
XM_017003193.1:c.2131C>G	XP_016858682.1:p.Leu711Val
NM_001320613.2:c.2857C>G	NP_001307542.1:p.Leu953Val
NM_001377128.1:c.2920C>G	NP_001364057.1:p.Leu974Val
NM_001377129.1:c.2716C>G	NP_001364058.1:p.Leu906Val
NM_001377130.1:c.2332-608C>G	NP_001364059.1:n.2332-608C>G
NM_001377131.1:c.2131C>G	NP_001364060.1:p.Leu711Val
NM_001377132.1:c.2854C>G	NP_001364061.1:p.Leu952Val
NM_004036.5:c.2854C>G MANE Select	NP_004027.2:p.Leu952Val