Canonical Allele Identifier: CA7489555

Gene: INO80

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41092132G>A , CM000677.2:g.41092132G>A	GRCh38
NC_000015.9:g.41384330G>A , CM000677.1:g.41384330G>A	GRCh37
NC_000015.8:g.39171622G>A	NCBI36
NG_017163.1:g.29011C>T
NG_017163.2:g.30647C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696949.1:c.432C>T	ENSP00000512991.1:p.Asp144=
ENST00000696954.1:n.1795C>T
ENST00000558357.6:c.432C>T	ENSP00000453677.1:p.Asp144=
ENST00000648947.1:c.432C>T MANE Select	ENSP00000497609.1:p.Asp144=
ENST00000361937.7:c.432C>T	ENSP00000355205.3:p.Asp144=
ENST00000401393.7:c.432C>T	ENSP00000384686.3:p.Asp144=
ENST00000558357.5:c.432C>T	ENSP00000453677.1:p.Asp144=
ENST00000616814.4:c.-3059C>T	ENSP00000483661.1:n.-3059C>T
NM_017553.2:c.432C>T	NP_060023.1:p.Asp144=
NR_104038.1:n.749C>T
XM_011521685.1:c.432C>T	XP_011519987.1:p.Asp144=
NM_017553.3:c.432C>T MANE Select	NP_060023.1:p.Asp144=
XM_011521685.3:c.432C>T	XP_011519987.1:p.Asp144=
XR_001751322.2:n.2281C>T
NR_104038.2:n.783C>T