Canonical Allele Identifier: CA379472732

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6636508C>A (hg19) ; chr11:g.6615277C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615277C>A , CM000673.2:g.6615277C>A	GRCh38
NC_000011.9:g.6636508C>A , CM000673.1:g.6636508C>A	GRCh37
NC_000011.8:g.6593084C>A	NCBI36
NG_008653.1:g.9185G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1205G>T	ENSP00000507321.1:p.Ser402Ile
ENST00000299427.12:c.1319G>T MANE Select	ENSP00000299427.6:p.Ser440Ile
ENST00000524611.2:n.179G>T
ENST00000524924.2:n.439G>T
ENST00000533371.6:c.590G>T	ENSP00000437066.1:p.Ser197Ile
ENST00000642892.1:c.590G>T	ENSP00000494165.1:p.Ser197Ile
ENST00000643342.1:c.392G>T
ENST00000643439.1:c.*1059G>T	ENSP00000495849.1:n.*1059G>T
ENST00000643479.1:n.1505G>T
ENST00000643516.1:c.828G>T
ENST00000644218.1:c.1130G>T	ENSP00000493574.1:p.Ser377Ile
ENST00000644683.1:c.*772G>T	ENSP00000494085.1:n.*772G>T
ENST00000644810.1:c.1040G>T	ENSP00000495895.1:p.Ser347Ile
ENST00000644831.1:n.1495G>T
ENST00000644933.1:c.*185G>T	ENSP00000496133.1:n.*185G>T
ENST00000645285.1:c.*185G>T	ENSP00000495058.1:n.*185G>T
ENST00000645331.1:n.2524G>T
ENST00000645620.1:c.590G>T	ENSP00000493657.1:p.Ser197Ile
ENST00000646691.1:n.1206G>T
ENST00000646777.1:n.1652G>T
ENST00000647016.1:n.1799G>T
ENST00000647152.1:c.590G>T	ENSP00000495893.1:p.Ser197Ile
ENST00000647209.1:c.*1188G>T	ENSP00000495558.1:n.*1188G>T
ENST00000647346.1:n.2339G>T
ENST00000299427.10:c.1319G>T	ENSP00000299427.6:p.Ser440Ile
ENST00000524611.1:n.197G>T
ENST00000524924.1:n.274G>T
ENST00000532191.1:n.372G>T
ENST00000533371.5:c.590G>T	ENSP00000437066.1:p.Ser197Ile
ENST00000611494.4:c.1319G>T	ENSP00000484546.1:p.Ser440Ile
NM_000391.3:c.1319G>T	NP_000382.3:p.Ser440Ile
NM_000391.4:c.1319G>T MANE Select	NP_000382.3:p.Ser440Ile