Canonical Allele Identifier: CA472922948

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638290G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617059G>C , CM000673.2:g.6617059G>C	GRCh38
NC_000011.9:g.6638290G>C , CM000673.1:g.6638290G>C	GRCh37
NC_000011.8:g.6594866G>C	NCBI36
NG_008653.1:g.7403C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.489C>G	ENSP00000507321.1:p.Thr163=
ENST00000299427.12:c.603C>G MANE Select	ENSP00000299427.6:p.Thr201=
ENST00000436873.7:c.312+242C>G
ENST00000524788.2:n.1762C>G
ENST00000524903.2:n.1878C>G
ENST00000528807.2:n.259C>G
ENST00000530040.2:n.479+300C>G
ENST00000533371.6:c.-127C>G	ENSP00000437066.1:n.-127C>G
ENST00000534644.6:n.551C>G
ENST00000642892.1:c.-127C>G	ENSP00000494165.1:n.-127C>G
ENST00000643439.1:c.*343C>G	ENSP00000495849.1:n.*343C>G
ENST00000643479.1:n.632C>G
ENST00000643516.1:c.395+242C>G
ENST00000644151.1:n.2042C>G
ENST00000644218.1:c.603C>G	ENSP00000493574.1:p.Thr201=
ENST00000644683.1:c.*56C>G	ENSP00000494085.1:n.*56C>G
ENST00000644810.1:c.324C>G	ENSP00000495895.1:p.Thr108=
ENST00000644831.1:n.779C>G
ENST00000644933.1:c.-127C>G	ENSP00000496133.1:n.-127C>G
ENST00000645020.1:n.1778C>G
ENST00000645285.1:c.-127C>G	ENSP00000495058.1:n.-127C>G
ENST00000645331.1:n.969C>G
ENST00000645620.1:c.-127C>G	ENSP00000493657.1:n.-127C>G
ENST00000646777.1:n.779C>G
ENST00000647016.1:n.1083C>G
ENST00000647152.1:c.-127C>G	ENSP00000495893.1:n.-127C>G
ENST00000647209.1:c.*472C>G	ENSP00000495558.1:n.*472C>G
ENST00000647346.1:n.1623C>G
ENST00000299427.10:c.603C>G	ENSP00000299427.6:p.Thr201=
ENST00000428886.6:n.772C>G
ENST00000436873.6:c.450+300C>G	ENSP00000398136.2:n.450+300C>G
ENST00000524788.1:n.303C>G
ENST00000528571.5:c.*343C>G	ENSP00000434647.1:n.*343C>G
ENST00000528807.1:n.153C>G
ENST00000533371.5:c.-127C>G	ENSP00000437066.1:n.-127C>G
ENST00000534644.5:n.588C>G
ENST00000611494.4:c.603C>G	ENSP00000484546.1:p.Thr201=
NM_000391.3:c.603C>G	NP_000382.3:p.Thr201=
NM_000391.4:c.603C>G MANE Select	NP_000382.3:p.Thr201=