Canonical Allele Identifier: CA379472226

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6635916A>T (hg19) ; chr11:g.6614685A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614685A>T , CM000673.2:g.6614685A>T	GRCh38
NC_000011.9:g.6635916A>T , CM000673.1:g.6635916A>T	GRCh37
NC_000011.8:g.6592492A>T	NCBI36
NG_008653.1:g.9777T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1439T>A	ENSP00000507321.1:p.Val480Glu
ENST00000299427.12:c.1553T>A MANE Select	ENSP00000299427.6:p.Val518Glu
ENST00000524611.2:n.592T>A
ENST00000524924.2:n.673T>A
ENST00000533371.6:c.824T>A	ENSP00000437066.1:p.Val275Glu
ENST00000642892.1:c.824T>A	ENSP00000494165.1:p.Val275Glu
ENST00000643342.1:c.626T>A
ENST00000643439.1:c.*1293T>A	ENSP00000495849.1:n.*1293T>A
ENST00000643479.1:n.1739T>A
ENST00000643516.1:c.1062T>A
ENST00000644218.1:c.1364T>A	ENSP00000493574.1:p.Val455Glu
ENST00000644683.1:c.*1006T>A	ENSP00000494085.1:n.*1006T>A
ENST00000644810.1:c.1274T>A	ENSP00000495895.1:p.Val425Glu
ENST00000644831.1:n.1729T>A
ENST00000644933.1:c.*419T>A	ENSP00000496133.1:n.*419T>A
ENST00000645285.1:c.*419T>A	ENSP00000495058.1:n.*419T>A
ENST00000645331.1:n.2758T>A
ENST00000645620.1:c.824T>A	ENSP00000493657.1:p.Val275Glu
ENST00000646691.1:n.1440T>A
ENST00000646777.1:n.1886T>A
ENST00000647016.1:n.2033T>A
ENST00000647152.1:c.824T>A	ENSP00000495893.1:p.Val275Glu
ENST00000647209.1:c.*1422T>A	ENSP00000495558.1:n.*1422T>A
ENST00000647346.1:n.2573T>A
ENST00000299427.10:c.1553T>A	ENSP00000299427.6:p.Val518Glu
ENST00000524611.1:n.431T>A
ENST00000533371.5:c.824T>A	ENSP00000437066.1:p.Val275Glu
ENST00000611494.4:c.1553T>A	ENSP00000484546.1:p.Val518Glu
NM_000391.3:c.1553T>A	NP_000382.3:p.Val518Glu
NM_000391.4:c.1553T>A MANE Select	NP_000382.3:p.Val518Glu