Canonical Allele Identifier: CA379475100

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638009C>G (hg19) ; chr11:g.6616778C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616778C>G , CM000673.2:g.6616778C>G	GRCh38
NC_000011.9:g.6638009C>G , CM000673.1:g.6638009C>G	GRCh37
NC_000011.8:g.6594585C>G	NCBI36
NG_008653.1:g.7684G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.655G>C	ENSP00000507321.1:p.Val219Leu
ENST00000299427.12:c.769G>C MANE Select	ENSP00000299427.6:p.Val257Leu
ENST00000436873.7:c.312+523G>C
ENST00000524788.2:n.1928G>C
ENST00000524903.2:n.2044G>C
ENST00000528807.2:n.425G>C
ENST00000530040.2:n.480-275G>C
ENST00000533371.6:c.40G>C	ENSP00000437066.1:p.Val14Leu
ENST00000642892.1:c.40G>C	ENSP00000494165.1:p.Val14Leu
ENST00000643439.1:c.*509G>C	ENSP00000495849.1:n.*509G>C
ENST00000643479.1:n.798G>C
ENST00000643516.1:c.396-275G>C
ENST00000644151.1:n.2208G>C
ENST00000644218.1:c.769G>C	ENSP00000493574.1:p.Val257Leu
ENST00000644683.1:c.*222G>C	ENSP00000494085.1:n.*222G>C
ENST00000644810.1:c.490G>C	ENSP00000495895.1:p.Val164Leu
ENST00000644831.1:n.945G>C
ENST00000644933.1:c.40G>C	ENSP00000496133.1:p.Val14Leu
ENST00000645020.1:n.2059G>C
ENST00000645285.1:c.40G>C	ENSP00000495058.1:p.Val14Leu
ENST00000645331.1:n.1135G>C
ENST00000645620.1:c.40G>C	ENSP00000493657.1:p.Val14Leu
ENST00000646777.1:n.945G>C
ENST00000647016.1:n.1249G>C
ENST00000647152.1:c.40G>C	ENSP00000495893.1:p.Val14Leu
ENST00000647209.1:c.*638G>C	ENSP00000495558.1:n.*638G>C
ENST00000647346.1:n.1789G>C
ENST00000299427.10:c.769G>C	ENSP00000299427.6:p.Val257Leu
ENST00000436873.6:c.451-275G>C	ENSP00000398136.2:n.451-275G>C
ENST00000524788.1:n.469G>C
ENST00000528807.1:n.319G>C
ENST00000533371.5:c.40G>C	ENSP00000437066.1:p.Val14Leu
ENST00000611494.4:c.769G>C	ENSP00000484546.1:p.Val257Leu
NM_000391.3:c.769G>C	NP_000382.3:p.Val257Leu
NM_000391.4:c.769G>C MANE Select	NP_000382.3:p.Val257Leu