Canonical Allele Identifier: CA472923009

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638937T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617706T>C , CM000673.2:g.6617706T>C	GRCh38
NC_000011.9:g.6638937T>C , CM000673.1:g.6638937T>C	GRCh37
NC_000011.8:g.6595513T>C	NCBI36
NG_008653.1:g.6756A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.186A>G	ENSP00000507321.1:p.Gln62=
ENST00000299427.12:c.300A>G MANE Select	ENSP00000299427.6:p.Gln100=
ENST00000428886.7:n.388A>G
ENST00000436873.7:c.104A>G
ENST00000524788.2:n.1312A>G
ENST00000524903.2:n.1428A>G
ENST00000528571.6:c.*40A>G	ENSP00000434647.1:n.*40A>G
ENST00000530040.2:n.329A>G
ENST00000533371.6:c.-430A>G	ENSP00000437066.1:n.-430A>G
ENST00000534644.6:n.301A>G
ENST00000642892.1:c.-377A>G	ENSP00000494165.1:n.-377A>G
ENST00000643439.1:c.*40A>G	ENSP00000495849.1:n.*40A>G
ENST00000643479.1:n.329A>G
ENST00000643516.1:c.187A>G
ENST00000644151.1:n.1592A>G
ENST00000644218.1:c.300A>G	ENSP00000493574.1:p.Gln100=
ENST00000644683.1:c.300A>G	ENSP00000494085.1:p.Gln100=
ENST00000644810.1:c.230-553A>G	ENSP00000495895.1:n.230-553A>G
ENST00000644831.1:n.329A>G
ENST00000644933.1:c.-430A>G	ENSP00000496133.1:n.-430A>G
ENST00000645020.1:n.1328A>G
ENST00000645285.1:c.-430A>G	ENSP00000495058.1:n.-430A>G
ENST00000645331.1:n.322A>G
ENST00000645620.1:c.-372A>G	ENSP00000493657.1:n.-372A>G
ENST00000646777.1:n.329A>G
ENST00000647016.1:n.633A>G
ENST00000647152.1:c.-430A>G	ENSP00000495893.1:n.-430A>G
ENST00000647209.1:c.*169A>G	ENSP00000495558.1:n.*169A>G
ENST00000647346.1:n.1320A>G
ENST00000299427.10:c.300A>G	ENSP00000299427.6:p.Gln100=
ENST00000428886.6:n.322A>G
ENST00000436873.6:c.300A>G	ENSP00000398136.2:p.Gln100=
ENST00000528571.5:c.*40A>G	ENSP00000434647.1:n.*40A>G
ENST00000530040.1:n.412A>G
ENST00000533371.5:c.-430A>G	ENSP00000437066.1:n.-430A>G
ENST00000534644.5:n.285A>G
ENST00000611494.4:c.300A>G	ENSP00000484546.1:p.Gln100=
NM_000391.3:c.300A>G	NP_000382.3:p.Gln100=
NM_000391.4:c.300A>G MANE Select	NP_000382.3:p.Gln100=