Canonical Allele Identifier: CA472922888

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638266G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617035G>A , CM000673.2:g.6617035G>A	GRCh38
NC_000011.9:g.6638266G>A , CM000673.1:g.6638266G>A	GRCh37
NC_000011.8:g.6594842G>A	NCBI36
NG_008653.1:g.7427C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.513C>T	ENSP00000507321.1:p.Tyr171=
ENST00000299427.12:c.627C>T MANE Select	ENSP00000299427.6:p.Tyr209=
ENST00000436873.7:c.312+266C>T
ENST00000524788.2:n.1786C>T
ENST00000524903.2:n.1902C>T
ENST00000528807.2:n.283C>T
ENST00000530040.2:n.479+324C>T
ENST00000533371.6:c.-103C>T	ENSP00000437066.1:n.-103C>T
ENST00000534644.6:n.575C>T
ENST00000642892.1:c.-103C>T	ENSP00000494165.1:n.-103C>T
ENST00000643439.1:c.*367C>T	ENSP00000495849.1:n.*367C>T
ENST00000643479.1:n.656C>T
ENST00000643516.1:c.395+266C>T
ENST00000644151.1:n.2066C>T
ENST00000644218.1:c.627C>T	ENSP00000493574.1:p.Tyr209=
ENST00000644683.1:c.*80C>T	ENSP00000494085.1:n.*80C>T
ENST00000644810.1:c.348C>T	ENSP00000495895.1:p.Tyr116=
ENST00000644831.1:n.803C>T
ENST00000644933.1:c.-103C>T	ENSP00000496133.1:n.-103C>T
ENST00000645020.1:n.1802C>T
ENST00000645285.1:c.-103C>T	ENSP00000495058.1:n.-103C>T
ENST00000645331.1:n.993C>T
ENST00000645620.1:c.-103C>T	ENSP00000493657.1:n.-103C>T
ENST00000646777.1:n.803C>T
ENST00000647016.1:n.1107C>T
ENST00000647152.1:c.-103C>T	ENSP00000495893.1:n.-103C>T
ENST00000647209.1:c.*496C>T	ENSP00000495558.1:n.*496C>T
ENST00000647346.1:n.1647C>T
ENST00000299427.10:c.627C>T	ENSP00000299427.6:p.Tyr209=
ENST00000428886.6:n.796C>T
ENST00000436873.6:c.450+324C>T	ENSP00000398136.2:n.450+324C>T
ENST00000524788.1:n.327C>T
ENST00000528571.5:c.*367C>T	ENSP00000434647.1:n.*367C>T
ENST00000528807.1:n.177C>T
ENST00000533371.5:c.-103C>T	ENSP00000437066.1:n.-103C>T
ENST00000534644.5:n.612C>T
ENST00000611494.4:c.627C>T	ENSP00000484546.1:p.Tyr209=
NM_000391.3:c.627C>T	NP_000382.3:p.Tyr209=
NM_000391.4:c.627C>T MANE Select	NP_000382.3:p.Tyr209=