Canonical Allele Identifier: CA472922851

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638236G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617005G>C , CM000673.2:g.6617005G>C	GRCh38
NC_000011.9:g.6638236G>C , CM000673.1:g.6638236G>C	GRCh37
NC_000011.8:g.6594812G>C	NCBI36
NG_008653.1:g.7457C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.543C>G	ENSP00000507321.1:p.Gly181=
ENST00000299427.12:c.657C>G MANE Select	ENSP00000299427.6:p.Gly219=
ENST00000436873.7:c.312+296C>G
ENST00000524788.2:n.1816C>G
ENST00000524903.2:n.1932C>G
ENST00000528807.2:n.313C>G
ENST00000530040.2:n.479+354C>G
ENST00000533371.6:c.-73C>G	ENSP00000437066.1:n.-73C>G
ENST00000534644.6:n.605C>G
ENST00000642892.1:c.-73C>G	ENSP00000494165.1:n.-73C>G
ENST00000643439.1:c.*397C>G	ENSP00000495849.1:n.*397C>G
ENST00000643479.1:n.686C>G
ENST00000643516.1:c.395+296C>G
ENST00000644151.1:n.2096C>G
ENST00000644218.1:c.657C>G	ENSP00000493574.1:p.Gly219=
ENST00000644683.1:c.*110C>G	ENSP00000494085.1:n.*110C>G
ENST00000644810.1:c.378C>G	ENSP00000495895.1:p.Gly126=
ENST00000644831.1:n.833C>G
ENST00000644933.1:c.-73C>G	ENSP00000496133.1:n.-73C>G
ENST00000645020.1:n.1832C>G
ENST00000645285.1:c.-73C>G	ENSP00000495058.1:n.-73C>G
ENST00000645331.1:n.1023C>G
ENST00000645620.1:c.-73C>G	ENSP00000493657.1:n.-73C>G
ENST00000646777.1:n.833C>G
ENST00000647016.1:n.1137C>G
ENST00000647152.1:c.-73C>G	ENSP00000495893.1:n.-73C>G
ENST00000647209.1:c.*526C>G	ENSP00000495558.1:n.*526C>G
ENST00000647346.1:n.1677C>G
ENST00000299427.10:c.657C>G	ENSP00000299427.6:p.Gly219=
ENST00000428886.6:n.826C>G
ENST00000436873.6:c.450+354C>G	ENSP00000398136.2:n.450+354C>G
ENST00000524788.1:n.357C>G
ENST00000528571.5:c.*397C>G	ENSP00000434647.1:n.*397C>G
ENST00000528807.1:n.207C>G
ENST00000533371.5:c.-73C>G	ENSP00000437066.1:n.-73C>G
ENST00000611494.4:c.657C>G	ENSP00000484546.1:p.Gly219=
NM_000391.3:c.657C>G	NP_000382.3:p.Gly219=
NM_000391.4:c.657C>G MANE Select	NP_000382.3:p.Gly219=