Canonical Allele Identifier: CA379475315

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638213C>T (hg19) ; chr11:g.6616982C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616982C>T , CM000673.2:g.6616982C>T	GRCh38
NC_000011.9:g.6638213C>T , CM000673.1:g.6638213C>T	GRCh37
NC_000011.8:g.6594789C>T	NCBI36
NG_008653.1:g.7480G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.566G>A	ENSP00000507321.1:p.Cys189Tyr
ENST00000299427.12:c.680G>A MANE Select	ENSP00000299427.6:p.Cys227Tyr
ENST00000436873.7:c.312+319G>A
ENST00000524788.2:n.1839G>A
ENST00000524903.2:n.1955G>A
ENST00000528807.2:n.336G>A
ENST00000530040.2:n.479+377G>A
ENST00000533371.6:c.-50G>A	ENSP00000437066.1:n.-50G>A
ENST00000534644.6:n.628G>A
ENST00000642892.1:c.-50G>A	ENSP00000494165.1:n.-50G>A
ENST00000643439.1:c.*420G>A	ENSP00000495849.1:n.*420G>A
ENST00000643479.1:n.709G>A
ENST00000643516.1:c.395+319G>A
ENST00000644151.1:n.2119G>A
ENST00000644218.1:c.680G>A	ENSP00000493574.1:p.Cys227Tyr
ENST00000644683.1:c.*133G>A	ENSP00000494085.1:n.*133G>A
ENST00000644810.1:c.401G>A	ENSP00000495895.1:p.Cys134Tyr
ENST00000644831.1:n.856G>A
ENST00000644933.1:c.-50G>A	ENSP00000496133.1:n.-50G>A
ENST00000645020.1:n.1855G>A
ENST00000645285.1:c.-50G>A	ENSP00000495058.1:n.-50G>A
ENST00000645331.1:n.1046G>A
ENST00000645620.1:c.-50G>A	ENSP00000493657.1:n.-50G>A
ENST00000646777.1:n.856G>A
ENST00000647016.1:n.1160G>A
ENST00000647152.1:c.-50G>A	ENSP00000495893.1:n.-50G>A
ENST00000647209.1:c.*549G>A	ENSP00000495558.1:n.*549G>A
ENST00000647346.1:n.1700G>A
ENST00000299427.10:c.680G>A	ENSP00000299427.6:p.Cys227Tyr
ENST00000436873.6:c.450+377G>A	ENSP00000398136.2:n.450+377G>A
ENST00000524788.1:n.380G>A
ENST00000528807.1:n.230G>A
ENST00000533371.5:c.-50G>A	ENSP00000437066.1:n.-50G>A
ENST00000611494.4:c.680G>A	ENSP00000484546.1:p.Cys227Tyr
NM_000391.3:c.680G>A	NP_000382.3:p.Cys227Tyr
NM_000391.4:c.680G>A MANE Select	NP_000382.3:p.Cys227Tyr