Canonical Allele Identifier: CA379475621

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638365A>C (hg19) ; chr11:g.6617134A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617134A>C , CM000673.2:g.6617134A>C	GRCh38
NC_000011.9:g.6638365A>C , CM000673.1:g.6638365A>C	GRCh37
NC_000011.8:g.6594941A>C	NCBI36
NG_008653.1:g.7328T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.414T>G	ENSP00000507321.1:p.Phe138Leu
ENST00000299427.12:c.528T>G MANE Select	ENSP00000299427.6:p.Phe176Leu
ENST00000428886.7:n.763T>G
ENST00000436873.7:c.312+167T>G
ENST00000524788.2:n.1687T>G
ENST00000524903.2:n.1803T>G
ENST00000528807.2:n.184T>G
ENST00000530040.2:n.479+225T>G
ENST00000533371.6:c.-202T>G	ENSP00000437066.1:n.-202T>G
ENST00000534644.6:n.476T>G
ENST00000642892.1:c.-202T>G	ENSP00000494165.1:n.-202T>G
ENST00000643439.1:c.*268T>G	ENSP00000495849.1:n.*268T>G
ENST00000643479.1:n.557T>G
ENST00000643516.1:c.395+167T>G
ENST00000644151.1:n.1967T>G
ENST00000644218.1:c.528T>G	ENSP00000493574.1:p.Phe176Leu
ENST00000644683.1:c.470T>G	ENSP00000494085.1:p.Phe157Cys
ENST00000644810.1:c.249T>G	ENSP00000495895.1:p.Phe83Leu
ENST00000644831.1:n.704T>G
ENST00000644933.1:c.-202T>G	ENSP00000496133.1:n.-202T>G
ENST00000645020.1:n.1703T>G
ENST00000645285.1:c.-202T>G	ENSP00000495058.1:n.-202T>G
ENST00000645331.1:n.894T>G
ENST00000645620.1:c.-202T>G	ENSP00000493657.1:n.-202T>G
ENST00000646777.1:n.704T>G
ENST00000647016.1:n.1008T>G
ENST00000647152.1:c.-202T>G	ENSP00000495893.1:n.-202T>G
ENST00000647209.1:c.*397T>G	ENSP00000495558.1:n.*397T>G
ENST00000647346.1:n.1548T>G
ENST00000299427.10:c.528T>G	ENSP00000299427.6:p.Phe176Leu
ENST00000428886.6:n.697T>G
ENST00000436873.6:c.450+225T>G	ENSP00000398136.2:n.450+225T>G
ENST00000524788.1:n.228T>G
ENST00000528571.5:c.*268T>G	ENSP00000434647.1:n.*268T>G
ENST00000528807.1:n.78T>G
ENST00000533371.5:c.-202T>G	ENSP00000437066.1:n.-202T>G
ENST00000534644.5:n.513T>G
ENST00000611494.4:c.528T>G	ENSP00000484546.1:p.Phe176Leu
NM_000391.3:c.528T>G	NP_000382.3:p.Phe176Leu
NM_000391.4:c.528T>G MANE Select	NP_000382.3:p.Phe176Leu