Canonical Allele Identifier: CA396396079

Gene: THAP11 CENPT

Linked Data

• MyVariant Identifiers: chr16:g.67876695T>C (hg19) ; chr16:g.67842792T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67842792T>C , CM000678.2:g.67842792T>C	GRCh38
NC_000016.9:g.67876695T>C , CM000678.1:g.67876695T>C	GRCh37
NC_000016.8:g.66434196T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303596.3:c.238T>C (THAP11) MANE Select	ENSP00000304689.1:p.Phe80Leu
ENST00000562787.6:c.-492+4609A>G (CENPT) MANE Select	ENSP00000457810.1:n.-492+4609A>G
ENST00000303596.2:c.238T>C (THAP11)	ENSP00000304689.1:p.Phe80Leu
ENST00000561593.5:c.-366+4788A>G (CENPT)	ENSP00000454481.1:n.-366+4788A>G
ENST00000562787.5:c.-492+4609A>G (CENPT)	ENSP00000457810.1:n.-492+4609A>G
ENST00000564144.5:n.348+166A>G (CENPT)
ENST00000564346.5:n.110+207A>G (CENPT)
ENST00000565114.5:c.-371+4788A>G (CENPT)	ENSP00000455638.1:n.-371+4788A>G
ENST00000565132.5:n.52+3980A>G (CENPT)
ENST00000565385.5:n.172+166A>G (CENPT)
ENST00000567482.5:n.260+239A>G (CENPT)
ENST00000567985.5:c.-371+166A>G (CENPT)	ENSP00000460542.1:n.-371+166A>G
ENST00000568652.5:n.173+4788A>G (CENPT)
ENST00000568765.5:n.232+4788A>G (CENPT)
ENST00000569019.5:n.339+207A>G (CENPT)
ENST00000569094.5:n.176+4788A>G (CENPT)
NM_020457.2:c.238T>C (THAP11)	NP_065190.2:p.Phe80Leu
NM_025082.3:c.-492+4609A>G (CENPT)	NP_079358.3:n.-492+4609A>G
NM_025082.4:c.-492+4609A>G (CENPT) MANE Select	NP_079358.3:n.-492+4609A>G
NM_020457.3:c.238T>C (THAP11) MANE Select	NP_065190.2:p.Phe80Leu