Canonical Allele Identifier: CA2241241391

Gene: CTU2

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88710834C>G , CM000678.2:g.88710834C>G	GRCh38
NC_000016.9:g.88777242C>G , CM000678.1:g.88777242C>G	GRCh37
NC_000016.8:g.87304743C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453996.7:c.282+552C>G MANE Select	ENSP00000388320.2:n.282+552C>G
ENST00000312060.9:c.282+552C>G	ENSP00000308617.5:n.282+552C>G
ENST00000453996.6:c.282+552C>G	ENSP00000388320.2:n.282+552C>G
ENST00000564105.5:c.203+552C>G	ENSP00000454923.1:n.203+552C>G
ENST00000564921.1:c.99+552C>G	ENSP00000455010.1:n.99+552C>G
ENST00000565071.1:n.820C>G
ENST00000566637.5:n.118+552C>G
ENST00000567949.5:c.282+552C>G	ENSP00000456908.1:n.282+552C>G
NM_001012759.1:c.282+552C>G	NP_001012777.1:n.282+552C>G
NM_001012762.1:c.282+552C>G	NP_001012780.1:n.282+552C>G
XM_011523068.1:c.21+552C>G	XP_011521370.1:n.21+552C>G
NM_001012759.2:c.282+552C>G	NP_001012777.1:n.282+552C>G
NM_001012762.2:c.282+552C>G	NP_001012780.1:n.282+552C>G
NM_001318507.1:c.282+552C>G	NP_001305436.1:n.282+552C>G
NM_001318513.1:c.21+552C>G	NP_001305442.1:n.21+552C>G
XM_017023210.2:c.-147+552C>G	XP_016878699.1:n.-147+552C>G
NM_001012759.3:c.282+552C>G MANE Select	NP_001012777.1:n.282+552C>G
NM_001012762.3:c.282+552C>G	NP_001012780.1:n.282+552C>G
NM_001318507.2:c.282+552C>G	NP_001305436.1:n.282+552C>G
NM_001318513.2:c.21+552C>G	NP_001305442.1:n.21+552C>G