Canonical Allele Identifier: CA346062828

Gene: ADCY3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2807T>C	ENSP00000384484.2:p.Phe936Ser
ENST00000679454.1:c.2804T>C MANE Select	ENSP00000505261.1:p.Phe935Ser
ENST00000260600.9:c.2804T>C	ENSP00000260600.5:p.Phe935Ser
ENST00000405392.5:c.2807T>C	ENSP00000384484.2:p.Phe936Ser
ENST00000485887.1:n.76T>C
ENST00000606682.5:c.1745T>C	ENSP00000475652.1:p.Phe582Ser
NM_004036.3:c.2804T>C	NP_004027.2:p.Phe935Ser
XM_005264104.1:c.2807T>C	XP_005264161.1:p.Phe936Ser
XM_005264105.1:c.2804T>C	XP_005264162.1:p.Phe935Ser
XM_006711925.1:c.2873T>C	XP_006711988.1:p.Phe958Ser
XM_011532489.1:c.2930T>C	XP_011530791.1:p.Phe977Ser
XM_011532490.1:c.2927T>C	XP_011530792.1:p.Phe976Ser
XM_011532491.1:c.2864T>C	XP_011530793.1:p.Phe955Ser
XM_011532492.1:c.2930T>C	XP_011530794.1:p.Phe977Ser
XM_011532493.1:c.2792T>C	XP_011530795.1:p.Phe931Ser
XM_011532494.1:c.2732T>C	XP_011530796.1:p.Phe911Ser
XM_011532495.1:c.2264T>C	XP_011530797.1:p.Phe755Ser
XM_011532496.1:c.2207T>C	XP_011530798.1:p.Phe736Ser
NM_001320613.1:c.2807T>C	NP_001307542.1:p.Phe936Ser
NM_004036.4:c.2804T>C	NP_004027.2:p.Phe935Ser
XM_011532492.2:c.2930T>C	XP_011530794.1:p.Phe977Ser
XM_017003186.1:c.2870T>C	XP_016858675.1:p.Phe957Ser
XM_017003187.1:c.2861T>C	XP_016858676.1:p.Phe954Ser
XM_017003188.1:c.2927T>C	XP_016858677.1:p.Phe976Ser
XM_017003189.1:c.2789T>C	XP_016858678.1:p.Phe930Ser
XM_017003190.1:c.2666T>C	XP_016858679.1:p.Phe889Ser
XM_017003191.1:c.2294T>C	XP_016858680.1:p.Phe765Ser
XM_017003192.1:c.2084T>C	XP_016858681.1:p.Phe695Ser
XM_017003193.1:c.2081T>C	XP_016858682.1:p.Phe694Ser
NM_001320613.2:c.2807T>C	NP_001307542.1:p.Phe936Ser
NM_001377128.1:c.2870T>C	NP_001364057.1:p.Phe957Ser
NM_001377129.1:c.2666T>C	NP_001364058.1:p.Phe889Ser
NM_001377130.1:c.2332-658T>C	NP_001364059.1:n.2332-658T>C
NM_001377131.1:c.2081T>C	NP_001364060.1:p.Phe694Ser
NM_001377132.1:c.2804T>C	NP_001364061.1:p.Phe935Ser
NM_004036.5:c.2804T>C MANE Select	NP_004027.2:p.Phe935Ser