Canonical Allele Identifier: CA425172185

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047328T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824459T>G , CM000664.2:g.24824459T>G	GRCh38
NC_000002.11:g.25047328T>G , CM000664.1:g.25047328T>G	GRCh37
NC_000002.10:g.24900832T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2658A>C	ENSP00000384484.2:p.Arg886=
ENST00000679454.1:c.2655A>C MANE Select	ENSP00000505261.1:p.Arg885=
ENST00000260600.9:c.2655A>C	ENSP00000260600.5:p.Arg885=
ENST00000405392.5:c.2658A>C	ENSP00000384484.2:p.Arg886=
ENST00000606682.5:c.1596A>C	ENSP00000475652.1:p.Arg532=
NM_004036.3:c.2655A>C	NP_004027.2:p.Arg885=
XM_005264104.1:c.2658A>C	XP_005264161.1:p.Arg886=
XM_005264105.1:c.2655A>C	XP_005264162.1:p.Arg885=
XM_006711925.1:c.2724A>C	XP_006711988.1:p.Arg908=
XM_011532489.1:c.2781A>C	XP_011530791.1:p.Arg927=
XM_011532490.1:c.2778A>C	XP_011530792.1:p.Arg926=
XM_011532491.1:c.2715A>C	XP_011530793.1:p.Arg905=
XM_011532492.1:c.2781A>C	XP_011530794.1:p.Arg927=
XM_011532493.1:c.2643A>C	XP_011530795.1:p.Arg881=
XM_011532494.1:c.2583A>C	XP_011530796.1:p.Arg861=
XM_011532495.1:c.2115A>C	XP_011530797.1:p.Arg705=
XM_011532496.1:c.2058A>C	XP_011530798.1:p.Arg686=
NM_001320613.1:c.2658A>C	NP_001307542.1:p.Arg886=
NM_004036.4:c.2655A>C	NP_004027.2:p.Arg885=
XM_011532492.2:c.2781A>C	XP_011530794.1:p.Arg927=
XM_017003186.1:c.2721A>C	XP_016858675.1:p.Arg907=
XM_017003187.1:c.2712A>C	XP_016858676.1:p.Arg904=
XM_017003188.1:c.2778A>C	XP_016858677.1:p.Arg926=
XM_017003189.1:c.2640A>C	XP_016858678.1:p.Arg880=
XM_017003190.1:c.2517A>C	XP_016858679.1:p.Arg839=
XM_017003191.1:c.2145A>C	XP_016858680.1:p.Arg715=
XM_017003192.1:c.1935A>C	XP_016858681.1:p.Arg645=
XM_017003193.1:c.1932A>C	XP_016858682.1:p.Arg644=
NM_001320613.2:c.2658A>C	NP_001307542.1:p.Arg886=
NM_001377128.1:c.2721A>C	NP_001364057.1:p.Arg907=
NM_001377129.1:c.2517A>C	NP_001364058.1:p.Arg839=
NM_001377130.1:c.2250A>C	NP_001364059.1:p.Arg750=
NM_001377131.1:c.1932A>C	NP_001364060.1:p.Arg644=
NM_001377132.1:c.2655A>C	NP_001364061.1:p.Arg885=
NM_004036.5:c.2655A>C MANE Select	NP_004027.2:p.Arg885=