Canonical Allele Identifier: CA472769006

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6635795C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614564C>T , CM000673.2:g.6614564C>T	GRCh38
NC_000011.9:g.6635795C>T , CM000673.1:g.6635795C>T	GRCh37
NC_000011.8:g.6592371C>T	NCBI36
NG_008653.1:g.9898G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1560G>A	ENSP00000507321.1:p.Lys520=
ENST00000299427.12:c.1674G>A MANE Select	ENSP00000299427.6:p.Lys558=
ENST00000524611.2:n.713G>A
ENST00000533371.6:c.945G>A	ENSP00000437066.1:p.Lys315=
ENST00000642892.1:c.945G>A	ENSP00000494165.1:p.Lys315=
ENST00000643342.1:c.747G>A
ENST00000643439.1:c.*1414G>A	ENSP00000495849.1:n.*1414G>A
ENST00000643479.1:n.1860G>A
ENST00000643516.1:c.1183G>A
ENST00000644218.1:c.1485G>A	ENSP00000493574.1:p.Lys495=
ENST00000644683.1:c.*1127G>A	ENSP00000494085.1:n.*1127G>A
ENST00000644810.1:c.1395G>A	ENSP00000495895.1:p.Lys465=
ENST00000644831.1:n.1850G>A
ENST00000644933.1:c.*540G>A	ENSP00000496133.1:n.*540G>A
ENST00000645285.1:c.*540G>A	ENSP00000495058.1:n.*540G>A
ENST00000645331.1:n.2879G>A
ENST00000645620.1:c.945G>A	ENSP00000493657.1:p.Lys315=
ENST00000646691.1:n.1561G>A
ENST00000646777.1:n.2007G>A
ENST00000647016.1:n.2154G>A
ENST00000647152.1:c.945G>A	ENSP00000495893.1:p.Lys315=
ENST00000647209.1:c.*1543G>A	ENSP00000495558.1:n.*1543G>A
ENST00000647346.1:n.2694G>A
ENST00000299427.10:c.1674G>A	ENSP00000299427.6:p.Lys558=
ENST00000533371.5:c.945G>A	ENSP00000437066.1:p.Lys315=
ENST00000611494.4:c.*2G>A	ENSP00000484546.1:n.*2G>A
NM_000391.3:c.1674G>A	NP_000382.3:p.Lys558=
NM_000391.4:c.1674G>A MANE Select	NP_000382.3:p.Lys558=