Canonical Allele Identifier: CA425171994

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046156G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823287G>A , CM000664.2:g.24823287G>A	GRCh38
NC_000002.11:g.25046156G>A , CM000664.1:g.25046156G>A	GRCh37
NC_000002.10:g.24899660G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2808C>T	ENSP00000384484.2:p.Phe936=
ENST00000679454.1:c.2805C>T MANE Select	ENSP00000505261.1:p.Phe935=
ENST00000260600.9:c.2805C>T	ENSP00000260600.5:p.Phe935=
ENST00000405392.5:c.2808C>T	ENSP00000384484.2:p.Phe936=
ENST00000485887.1:n.77C>T
ENST00000606682.5:c.1746C>T	ENSP00000475652.1:p.Phe582=
NM_004036.3:c.2805C>T	NP_004027.2:p.Phe935=
XM_005264104.1:c.2808C>T	XP_005264161.1:p.Phe936=
XM_005264105.1:c.2805C>T	XP_005264162.1:p.Phe935=
XM_006711925.1:c.2874C>T	XP_006711988.1:p.Phe958=
XM_011532489.1:c.2931C>T	XP_011530791.1:p.Phe977=
XM_011532490.1:c.2928C>T	XP_011530792.1:p.Phe976=
XM_011532491.1:c.2865C>T	XP_011530793.1:p.Phe955=
XM_011532492.1:c.2931C>T	XP_011530794.1:p.Phe977=
XM_011532493.1:c.2793C>T	XP_011530795.1:p.Phe931=
XM_011532494.1:c.2733C>T	XP_011530796.1:p.Phe911=
XM_011532495.1:c.2265C>T	XP_011530797.1:p.Phe755=
XM_011532496.1:c.2208C>T	XP_011530798.1:p.Phe736=
NM_001320613.1:c.2808C>T	NP_001307542.1:p.Phe936=
NM_004036.4:c.2805C>T	NP_004027.2:p.Phe935=
XM_011532492.2:c.2931C>T	XP_011530794.1:p.Phe977=
XM_017003186.1:c.2871C>T	XP_016858675.1:p.Phe957=
XM_017003187.1:c.2862C>T	XP_016858676.1:p.Phe954=
XM_017003188.1:c.2928C>T	XP_016858677.1:p.Phe976=
XM_017003189.1:c.2790C>T	XP_016858678.1:p.Phe930=
XM_017003190.1:c.2667C>T	XP_016858679.1:p.Phe889=
XM_017003191.1:c.2295C>T	XP_016858680.1:p.Phe765=
XM_017003192.1:c.2085C>T	XP_016858681.1:p.Phe695=
XM_017003193.1:c.2082C>T	XP_016858682.1:p.Phe694=
NM_001320613.2:c.2808C>T	NP_001307542.1:p.Phe936=
NM_001377128.1:c.2871C>T	NP_001364057.1:p.Phe957=
NM_001377129.1:c.2667C>T	NP_001364058.1:p.Phe889=
NM_001377130.1:c.2332-657C>T	NP_001364059.1:n.2332-657C>T
NM_001377131.1:c.2082C>T	NP_001364060.1:p.Phe694=
NM_001377132.1:c.2805C>T	NP_001364061.1:p.Phe935=
NM_004036.5:c.2805C>T MANE Select	NP_004027.2:p.Phe935=