Canonical Allele Identifier: CA7488762

Gene: INO80

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41016167A>C , CM000677.2:g.41016167A>C	GRCh38
NC_000015.9:g.41308365A>C , CM000677.1:g.41308365A>C	GRCh37
NC_000015.8:g.39095657A>C	NCBI36
NG_017163.1:g.104976T>G
NG_017163.2:g.106612T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558270.2:n.1262T>G
ENST00000696949.1:c.*1212T>G	ENSP00000512991.1:n.*1212T>G
ENST00000696950.1:n.2900T>G
ENST00000558357.6:c.3274+4733T>G	ENSP00000453677.1:n.3274+4733T>G
ENST00000559995.2:c.1262T>G	ENSP00000454057.2:n.1262T>G
ENST00000648947.1:c.3323T>G MANE Select	ENSP00000497609.1:p.Val1108Gly
ENST00000361937.7:c.3323T>G	ENSP00000355205.3:p.Val1108Gly
ENST00000401393.7:c.3323T>G	ENSP00000384686.3:p.Val1108Gly
ENST00000557849.1:c.400T>G
ENST00000558357.5:c.3274+4733T>G	ENSP00000453677.1:n.3274+4733T>G
ENST00000616814.4:c.-217+4733T>G	ENSP00000483661.1:n.-217+4733T>G
NM_017553.2:c.3323T>G	NP_060023.1:p.Val1108Gly
NR_104038.1:n.3591+4733T>G
XM_011521685.1:c.3323T>G	XP_011519987.1:p.Val1108Gly
XM_011521686.1:c.1373T>G	XP_011519988.1:p.Val458Gly
NM_017553.3:c.3323T>G MANE Select	NP_060023.1:p.Val1108Gly
XM_011521685.3:c.3323T>G	XP_011519987.1:p.Val1108Gly
XM_011521686.3:c.1373T>G	XP_011519988.1:p.Val458Gly
XR_001751322.2:n.5123+4733T>G
NR_104038.2:n.3625+4733T>G