Canonical Allele Identifier: CA8230972

Gene: CTU2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88714632A>G , CM000678.2:g.88714632A>G	GRCh38
NC_000016.9:g.88781040A>G , CM000678.1:g.88781040A>G	GRCh37
NC_000016.8:g.87308541A>G	NCBI36
NG_042229.1:g.75589T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453996.7:c.1247A>G MANE Select	ENSP00000388320.2:p.Gln416Arg
ENST00000312060.9:c.1247A>G	ENSP00000308617.5:p.Gln416Arg
ENST00000453996.6:c.1247A>G	ENSP00000388320.2:p.Gln416Arg
ENST00000564105.5:c.*958A>G	ENSP00000454923.1:n.*958A>G
ENST00000564584.1:n.541A>G
ENST00000566637.5:n.1183A>G
ENST00000567949.5:c.1460A>G	ENSP00000456908.1:p.Gln487Arg
NM_001012759.1:c.1247A>G	NP_001012777.1:p.Gln416Arg
NM_001012762.1:c.1247A>G	NP_001012780.1:p.Gln416Arg
XM_011523068.1:c.986A>G	XP_011521370.1:p.Gln329Arg
NM_001012759.2:c.1247A>G	NP_001012777.1:p.Gln416Arg
NM_001012762.2:c.1247A>G	NP_001012780.1:p.Gln416Arg
NM_001318507.1:c.1460A>G	NP_001305436.1:p.Gln487Arg
NM_001318513.1:c.986A>G	NP_001305442.1:p.Gln329Arg
XM_017023210.2:c.797A>G	XP_016878699.1:p.Gln266Arg
NM_001012759.3:c.1247A>G MANE Select	NP_001012777.1:p.Gln416Arg
NM_001012762.3:c.1247A>G	NP_001012780.1:p.Gln416Arg
NM_001318507.2:c.1460A>G	NP_001305436.1:p.Gln487Arg
NM_001318513.2:c.986A>G	NP_001305442.1:p.Gln329Arg