Canonical Allele Identifier: CA379475082

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6637997C>A (hg19) ; chr11:g.6616766C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616766C>A , CM000673.2:g.6616766C>A	GRCh38
NC_000011.9:g.6637997C>A , CM000673.1:g.6637997C>A	GRCh37
NC_000011.8:g.6594573C>A	NCBI36
NG_008653.1:g.7696G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.667G>T	ENSP00000507321.1:p.Val223Phe
ENST00000299427.12:c.781G>T MANE Select	ENSP00000299427.6:p.Val261Phe
ENST00000436873.7:c.312+535G>T
ENST00000524788.2:n.1940G>T
ENST00000524903.2:n.2056G>T
ENST00000528807.2:n.437G>T
ENST00000530040.2:n.480-263G>T
ENST00000533371.6:c.52G>T	ENSP00000437066.1:p.Val18Phe
ENST00000642892.1:c.52G>T	ENSP00000494165.1:p.Val18Phe
ENST00000643439.1:c.*521G>T	ENSP00000495849.1:n.*521G>T
ENST00000643479.1:n.810G>T
ENST00000643516.1:c.396-263G>T
ENST00000644151.1:n.2220G>T
ENST00000644218.1:c.781G>T	ENSP00000493574.1:p.Val261Phe
ENST00000644683.1:c.*234G>T	ENSP00000494085.1:n.*234G>T
ENST00000644810.1:c.502G>T	ENSP00000495895.1:p.Val168Phe
ENST00000644831.1:n.957G>T
ENST00000644933.1:c.52G>T	ENSP00000496133.1:p.Val18Phe
ENST00000645020.1:n.2071G>T
ENST00000645285.1:c.52G>T	ENSP00000495058.1:p.Val18Phe
ENST00000645331.1:n.1147G>T
ENST00000645620.1:c.52G>T	ENSP00000493657.1:p.Val18Phe
ENST00000646777.1:n.957G>T
ENST00000647016.1:n.1261G>T
ENST00000647152.1:c.52G>T	ENSP00000495893.1:p.Val18Phe
ENST00000647209.1:c.*650G>T	ENSP00000495558.1:n.*650G>T
ENST00000647346.1:n.1801G>T
ENST00000299427.10:c.781G>T	ENSP00000299427.6:p.Val261Phe
ENST00000436873.6:c.451-263G>T	ENSP00000398136.2:n.451-263G>T
ENST00000524788.1:n.481G>T
ENST00000528807.1:n.331G>T
ENST00000533371.5:c.52G>T	ENSP00000437066.1:p.Val18Phe
ENST00000611494.4:c.781G>T	ENSP00000484546.1:p.Val261Phe
NM_000391.3:c.781G>T	NP_000382.3:p.Val261Phe
NM_000391.4:c.781G>T MANE Select	NP_000382.3:p.Val261Phe