Canonical Allele Identifier: CA346062827

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046157A>C (hg19) ; chr2:g.24823288A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823288A>C , CM000664.2:g.24823288A>C	GRCh38
NC_000002.11:g.25046157A>C , CM000664.1:g.25046157A>C	GRCh37
NC_000002.10:g.24899661A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2807T>G	ENSP00000384484.2:p.Phe936Cys
ENST00000679454.1:c.2804T>G MANE Select	ENSP00000505261.1:p.Phe935Cys
ENST00000260600.9:c.2804T>G	ENSP00000260600.5:p.Phe935Cys
ENST00000405392.5:c.2807T>G	ENSP00000384484.2:p.Phe936Cys
ENST00000485887.1:n.76T>G
ENST00000606682.5:c.1745T>G	ENSP00000475652.1:p.Phe582Cys
NM_004036.3:c.2804T>G	NP_004027.2:p.Phe935Cys
XM_005264104.1:c.2807T>G	XP_005264161.1:p.Phe936Cys
XM_005264105.1:c.2804T>G	XP_005264162.1:p.Phe935Cys
XM_006711925.1:c.2873T>G	XP_006711988.1:p.Phe958Cys
XM_011532489.1:c.2930T>G	XP_011530791.1:p.Phe977Cys
XM_011532490.1:c.2927T>G	XP_011530792.1:p.Phe976Cys
XM_011532491.1:c.2864T>G	XP_011530793.1:p.Phe955Cys
XM_011532492.1:c.2930T>G	XP_011530794.1:p.Phe977Cys
XM_011532493.1:c.2792T>G	XP_011530795.1:p.Phe931Cys
XM_011532494.1:c.2732T>G	XP_011530796.1:p.Phe911Cys
XM_011532495.1:c.2264T>G	XP_011530797.1:p.Phe755Cys
XM_011532496.1:c.2207T>G	XP_011530798.1:p.Phe736Cys
NM_001320613.1:c.2807T>G	NP_001307542.1:p.Phe936Cys
NM_004036.4:c.2804T>G	NP_004027.2:p.Phe935Cys
XM_011532492.2:c.2930T>G	XP_011530794.1:p.Phe977Cys
XM_017003186.1:c.2870T>G	XP_016858675.1:p.Phe957Cys
XM_017003187.1:c.2861T>G	XP_016858676.1:p.Phe954Cys
XM_017003188.1:c.2927T>G	XP_016858677.1:p.Phe976Cys
XM_017003189.1:c.2789T>G	XP_016858678.1:p.Phe930Cys
XM_017003190.1:c.2666T>G	XP_016858679.1:p.Phe889Cys
XM_017003191.1:c.2294T>G	XP_016858680.1:p.Phe765Cys
XM_017003192.1:c.2084T>G	XP_016858681.1:p.Phe695Cys
XM_017003193.1:c.2081T>G	XP_016858682.1:p.Phe694Cys
NM_001320613.2:c.2807T>G	NP_001307542.1:p.Phe936Cys
NM_001377128.1:c.2870T>G	NP_001364057.1:p.Phe957Cys
NM_001377129.1:c.2666T>G	NP_001364058.1:p.Phe889Cys
NM_001377130.1:c.2332-658T>G	NP_001364059.1:n.2332-658T>G
NM_001377131.1:c.2081T>G	NP_001364060.1:p.Phe694Cys
NM_001377132.1:c.2804T>G	NP_001364061.1:p.Phe935Cys
NM_004036.5:c.2804T>G MANE Select	NP_004027.2:p.Phe935Cys