Canonical Allele Identifier: CA379475733

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638561G>C (hg19) ; chr11:g.6617330G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617330G>C , CM000673.2:g.6617330G>C	GRCh38
NC_000011.9:g.6638561G>C , CM000673.1:g.6638561G>C	GRCh37
NC_000011.8:g.6595137G>C	NCBI36
NG_008653.1:g.7132C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.365C>G	ENSP00000507321.1:p.Pro122Arg
ENST00000299427.12:c.479C>G MANE Select	ENSP00000299427.6:p.Pro160Arg
ENST00000428886.7:n.567C>G
ENST00000436873.7:c.283C>G
ENST00000524788.2:n.1491C>G
ENST00000524903.2:n.1607C>G
ENST00000528571.6:c.*219C>G	ENSP00000434647.1:n.*219C>G
ENST00000528807.2:n.135C>G
ENST00000530040.2:n.479+29C>G
ENST00000533371.6:c.-251C>G	ENSP00000437066.1:n.-251C>G
ENST00000534644.6:n.456+24C>G
ENST00000642892.1:c.-222+24C>G	ENSP00000494165.1:n.-222+24C>G
ENST00000643439.1:c.*219C>G	ENSP00000495849.1:n.*219C>G
ENST00000643479.1:n.508C>G
ENST00000643516.1:c.366C>G
ENST00000644151.1:n.1771C>G
ENST00000644218.1:c.479C>G	ENSP00000493574.1:p.Pro160Arg
ENST00000644683.1:c.450+29C>G	ENSP00000494085.1:n.450+29C>G
ENST00000644810.1:c.230-177C>G	ENSP00000495895.1:n.230-177C>G
ENST00000644831.1:n.508C>G
ENST00000644933.1:c.-251C>G	ENSP00000496133.1:n.-251C>G
ENST00000645020.1:n.1507C>G
ENST00000645285.1:c.-251C>G	ENSP00000495058.1:n.-251C>G
ENST00000645331.1:n.698C>G
ENST00000645620.1:c.-222+29C>G	ENSP00000493657.1:n.-222+29C>G
ENST00000646777.1:n.508C>G
ENST00000647016.1:n.812C>G
ENST00000647152.1:c.-251C>G	ENSP00000495893.1:n.-251C>G
ENST00000647209.1:c.*348C>G	ENSP00000495558.1:n.*348C>G
ENST00000647346.1:n.1499C>G
ENST00000299427.10:c.479C>G	ENSP00000299427.6:p.Pro160Arg
ENST00000428886.6:n.501C>G
ENST00000436873.6:c.450+29C>G	ENSP00000398136.2:n.450+29C>G
ENST00000524788.1:n.32C>G
ENST00000528571.5:c.*219C>G	ENSP00000434647.1:n.*219C>G
ENST00000533371.5:c.-251C>G	ENSP00000437066.1:n.-251C>G
ENST00000534644.5:n.464C>G
ENST00000611494.4:c.479C>G	ENSP00000484546.1:p.Pro160Arg
NM_000391.3:c.479C>G	NP_000382.3:p.Pro160Arg
NM_000391.4:c.479C>G MANE Select	NP_000382.3:p.Pro160Arg