Canonical Allele Identifier: CA7488963

Gene: INO80

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41047499T>C , CM000677.2:g.41047499T>C	GRCh38
NC_000015.9:g.41339697T>C , CM000677.1:g.41339697T>C	GRCh37
NC_000015.8:g.39126989T>C	NCBI36
NG_017163.1:g.73644A>G
NG_017163.2:g.75280A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558270.2:n.809A>G
ENST00000696949.1:c.*533A>G	ENSP00000512991.1:n.*533A>G
ENST00000696952.1:n.746A>G
ENST00000558357.6:c.2644A>G	ENSP00000453677.1:p.Ile882Val
ENST00000559995.2:c.809A>G	ENSP00000454057.2:n.809A>G
ENST00000648947.1:c.2644A>G MANE Select	ENSP00000497609.1:p.Ile882Val
ENST00000361937.7:c.2644A>G	ENSP00000355205.3:p.Ile882Val
ENST00000401393.7:c.2644A>G	ENSP00000384686.3:p.Ile882Val
ENST00000558357.5:c.2644A>G	ENSP00000453677.1:p.Ile882Val
ENST00000616814.4:c.-847A>G	ENSP00000483661.1:n.-847A>G
NM_017553.2:c.2644A>G	NP_060023.1:p.Ile882Val
NR_104038.1:n.2961A>G
XM_011521685.1:c.2644A>G	XP_011519987.1:p.Ile882Val
XM_011521686.1:c.694A>G	XP_011519988.1:p.Ile232Val
NM_017553.3:c.2644A>G MANE Select	NP_060023.1:p.Ile882Val
XM_011521685.3:c.2644A>G	XP_011519987.1:p.Ile882Val
XM_011521686.3:c.694A>G	XP_011519988.1:p.Ile232Val
XR_001751322.2:n.4493A>G
NR_104038.2:n.2995A>G