Canonical Allele Identifier: CA7488520

Gene: INO80

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40983837C>G , CM000677.2:g.40983837C>G	GRCh38
NC_000015.9:g.41276035C>G , CM000677.1:g.41276035C>G	GRCh37
NC_000015.8:g.39063327C>G	NCBI36
NG_017163.1:g.137306G>C
NG_017163.2:g.138942G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558270.2:n.2101G>C
ENST00000560799.6:n.1054G>C
ENST00000696947.1:n.1217G>C
ENST00000696948.1:n.993G>C
ENST00000696949.1:c.*2051G>C	ENSP00000512991.1:n.*2051G>C
ENST00000558357.6:c.*719G>C	ENSP00000453677.1:n.*719G>C
ENST00000559995.2:c.2101G>C	ENSP00000454057.2:n.2101G>C
ENST00000648947.1:c.4162G>C MANE Select	ENSP00000497609.1:p.Ala1388Pro
ENST00000361937.7:c.4162G>C	ENSP00000355205.3:p.Ala1388Pro
ENST00000401393.7:c.4162G>C	ENSP00000384686.3:p.Ala1388Pro
ENST00000558357.5:c.*719G>C	ENSP00000453677.1:n.*719G>C
ENST00000560689.1:n.150G>C
ENST00000616814.4:c.515+29G>C	ENSP00000483661.1:n.515+29G>C
NM_017553.2:c.4162G>C	NP_060023.1:p.Ala1388Pro
NR_104038.1:n.4351G>C
XM_011521686.1:c.2212G>C	XP_011519988.1:p.Ala738Pro
NM_017553.3:c.4162G>C MANE Select	NP_060023.1:p.Ala1388Pro
XM_011521686.3:c.2212G>C	XP_011519988.1:p.Ala738Pro
NR_104038.2:n.4385G>C