Canonical Allele Identifier: CA379476020

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638637C>A (hg19) ; chr11:g.6617406C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617406C>A , CM000673.2:g.6617406C>A	GRCh38
NC_000011.9:g.6638637C>A , CM000673.1:g.6638637C>A	GRCh37
NC_000011.8:g.6595213C>A	NCBI36
NG_008653.1:g.7056G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.289G>T	ENSP00000507321.1:p.Gly97Trp
ENST00000299427.12:c.403G>T MANE Select	ENSP00000299427.6:p.Gly135Trp
ENST00000428886.7:n.491G>T
ENST00000436873.7:c.207G>T
ENST00000524788.2:n.1415G>T
ENST00000524903.2:n.1531G>T
ENST00000528571.6:c.*143G>T	ENSP00000434647.1:n.*143G>T
ENST00000528807.2:n.59G>T
ENST00000530040.2:n.432G>T
ENST00000533371.6:c.-327G>T	ENSP00000437066.1:n.-327G>T
ENST00000534644.6:n.404G>T
ENST00000642892.1:c.-274G>T	ENSP00000494165.1:n.-274G>T
ENST00000643439.1:c.*143G>T	ENSP00000495849.1:n.*143G>T
ENST00000643479.1:n.432G>T
ENST00000643516.1:c.290G>T
ENST00000644151.1:n.1695G>T
ENST00000644218.1:c.403G>T	ENSP00000493574.1:p.Gly135Trp
ENST00000644683.1:c.403G>T	ENSP00000494085.1:p.Gly135Trp
ENST00000644810.1:c.230-253G>T	ENSP00000495895.1:n.230-253G>T
ENST00000644831.1:n.432G>T
ENST00000644933.1:c.-327G>T	ENSP00000496133.1:n.-327G>T
ENST00000645020.1:n.1431G>T
ENST00000645285.1:c.-327G>T	ENSP00000495058.1:n.-327G>T
ENST00000645331.1:n.622G>T
ENST00000645620.1:c.-269G>T	ENSP00000493657.1:n.-269G>T
ENST00000646777.1:n.432G>T
ENST00000647016.1:n.736G>T
ENST00000647152.1:c.-327G>T	ENSP00000495893.1:n.-327G>T
ENST00000647209.1:c.*272G>T	ENSP00000495558.1:n.*272G>T
ENST00000647346.1:n.1423G>T
ENST00000299427.10:c.403G>T	ENSP00000299427.6:p.Gly135Trp
ENST00000428886.6:n.425G>T
ENST00000436873.6:c.403G>T	ENSP00000398136.2:p.Gly135Trp
ENST00000528571.5:c.*143G>T	ENSP00000434647.1:n.*143G>T
ENST00000530040.1:n.515G>T
ENST00000533371.5:c.-327G>T	ENSP00000437066.1:n.-327G>T
ENST00000534644.5:n.388G>T
ENST00000611494.4:c.403G>T	ENSP00000484546.1:p.Gly135Trp
NM_000391.3:c.403G>T	NP_000382.3:p.Gly135Trp
NM_000391.4:c.403G>T MANE Select	NP_000382.3:p.Gly135Trp