Canonical Allele Identifier: CA379476126

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638860A>G (hg19) ; chr11:g.6617629A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617629A>G , CM000673.2:g.6617629A>G	GRCh38
NC_000011.9:g.6638860A>G , CM000673.1:g.6638860A>G	GRCh37
NC_000011.8:g.6595436A>G	NCBI36
NG_008653.1:g.6833T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.263T>C	ENSP00000507321.1:p.Ile88Thr
ENST00000299427.12:c.377T>C MANE Select	ENSP00000299427.6:p.Ile126Thr
ENST00000428886.7:n.465T>C
ENST00000436873.7:c.181T>C
ENST00000524788.2:n.1389T>C
ENST00000524903.2:n.1505T>C
ENST00000528571.6:c.*117T>C	ENSP00000434647.1:n.*117T>C
ENST00000530040.2:n.406T>C
ENST00000533371.6:c.-353T>C	ENSP00000437066.1:n.-353T>C
ENST00000534644.6:n.378T>C
ENST00000642892.1:c.-300T>C	ENSP00000494165.1:n.-300T>C
ENST00000643439.1:c.*117T>C	ENSP00000495849.1:n.*117T>C
ENST00000643479.1:n.406T>C
ENST00000643516.1:c.264T>C
ENST00000644151.1:n.1669T>C
ENST00000644218.1:c.377T>C	ENSP00000493574.1:p.Ile126Thr
ENST00000644683.1:c.377T>C	ENSP00000494085.1:p.Ile126Thr
ENST00000644810.1:c.230-476T>C	ENSP00000495895.1:n.230-476T>C
ENST00000644831.1:n.406T>C
ENST00000644933.1:c.-353T>C	ENSP00000496133.1:n.-353T>C
ENST00000645020.1:n.1405T>C
ENST00000645285.1:c.-353T>C	ENSP00000495058.1:n.-353T>C
ENST00000645331.1:n.399T>C
ENST00000645620.1:c.-295T>C	ENSP00000493657.1:n.-295T>C
ENST00000646777.1:n.406T>C
ENST00000647016.1:n.710T>C
ENST00000647152.1:c.-353T>C	ENSP00000495893.1:n.-353T>C
ENST00000647209.1:c.*246T>C	ENSP00000495558.1:n.*246T>C
ENST00000647346.1:n.1397T>C
ENST00000299427.10:c.377T>C	ENSP00000299427.6:p.Ile126Thr
ENST00000428886.6:n.399T>C
ENST00000436873.6:c.377T>C	ENSP00000398136.2:p.Ile126Thr
ENST00000528571.5:c.*117T>C	ENSP00000434647.1:n.*117T>C
ENST00000530040.1:n.489T>C
ENST00000533371.5:c.-353T>C	ENSP00000437066.1:n.-353T>C
ENST00000534644.5:n.362T>C
ENST00000611494.4:c.377T>C	ENSP00000484546.1:p.Ile126Thr
NM_000391.3:c.377T>C	NP_000382.3:p.Ile126Thr
NM_000391.4:c.377T>C MANE Select	NP_000382.3:p.Ile126Thr