Canonical Allele Identifier: CA379475001

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6637954A>G (hg19) ; chr11:g.6616723A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616723A>G , CM000673.2:g.6616723A>G	GRCh38
NC_000011.9:g.6637954A>G , CM000673.1:g.6637954A>G	GRCh37
NC_000011.8:g.6594530A>G	NCBI36
NG_008653.1:g.7739T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.710T>C	ENSP00000507321.1:p.Leu237Pro
ENST00000299427.12:c.824T>C MANE Select	ENSP00000299427.6:p.Leu275Pro
ENST00000436873.7:c.312+578T>C
ENST00000524788.2:n.1983T>C
ENST00000524903.2:n.2099T>C
ENST00000528807.2:n.480T>C
ENST00000530040.2:n.480-220T>C
ENST00000533371.6:c.95T>C	ENSP00000437066.1:p.Leu32Pro
ENST00000642892.1:c.95T>C	ENSP00000494165.1:p.Leu32Pro
ENST00000643439.1:c.*564T>C	ENSP00000495849.1:n.*564T>C
ENST00000643479.1:n.853T>C
ENST00000643516.1:c.396-220T>C
ENST00000644151.1:n.2263T>C
ENST00000644218.1:c.824T>C	ENSP00000493574.1:p.Leu275Pro
ENST00000644683.1:c.*277T>C	ENSP00000494085.1:n.*277T>C
ENST00000644810.1:c.545T>C	ENSP00000495895.1:p.Leu182Pro
ENST00000644831.1:n.1000T>C
ENST00000644933.1:c.95T>C	ENSP00000496133.1:p.Leu32Pro
ENST00000645020.1:n.2114T>C
ENST00000645285.1:c.95T>C	ENSP00000495058.1:p.Leu32Pro
ENST00000645331.1:n.1190T>C
ENST00000645620.1:c.95T>C	ENSP00000493657.1:p.Leu32Pro
ENST00000646777.1:n.1000T>C
ENST00000647016.1:n.1304T>C
ENST00000647152.1:c.95T>C	ENSP00000495893.1:p.Leu32Pro
ENST00000647209.1:c.*693T>C	ENSP00000495558.1:n.*693T>C
ENST00000647346.1:n.1844T>C
ENST00000299427.10:c.824T>C	ENSP00000299427.6:p.Leu275Pro
ENST00000436873.6:c.451-220T>C	ENSP00000398136.2:n.451-220T>C
ENST00000524788.1:n.524T>C
ENST00000528807.1:n.374T>C
ENST00000533371.5:c.95T>C	ENSP00000437066.1:p.Leu32Pro
ENST00000611494.4:c.824T>C	ENSP00000484546.1:p.Leu275Pro
NM_000391.3:c.824T>C	NP_000382.3:p.Leu275Pro
NM_000391.4:c.824T>C MANE Select	NP_000382.3:p.Leu275Pro