Canonical Allele Identifier: CA379475047

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6637979C>A (hg19) ; chr11:g.6616748C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616748C>A , CM000673.2:g.6616748C>A	GRCh38
NC_000011.9:g.6637979C>A , CM000673.1:g.6637979C>A	GRCh37
NC_000011.8:g.6594555C>A	NCBI36
NG_008653.1:g.7714G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.685G>T	ENSP00000507321.1:p.Gly229Cys
ENST00000299427.12:c.799G>T MANE Select	ENSP00000299427.6:p.Gly267Cys
ENST00000436873.7:c.312+553G>T
ENST00000524788.2:n.1958G>T
ENST00000524903.2:n.2074G>T
ENST00000528807.2:n.455G>T
ENST00000530040.2:n.480-245G>T
ENST00000533371.6:c.70G>T	ENSP00000437066.1:p.Gly24Cys
ENST00000642892.1:c.70G>T	ENSP00000494165.1:p.Gly24Cys
ENST00000643439.1:c.*539G>T	ENSP00000495849.1:n.*539G>T
ENST00000643479.1:n.828G>T
ENST00000643516.1:c.396-245G>T
ENST00000644151.1:n.2238G>T
ENST00000644218.1:c.799G>T	ENSP00000493574.1:p.Gly267Cys
ENST00000644683.1:c.*252G>T	ENSP00000494085.1:n.*252G>T
ENST00000644810.1:c.520G>T	ENSP00000495895.1:p.Gly174Cys
ENST00000644831.1:n.975G>T
ENST00000644933.1:c.70G>T	ENSP00000496133.1:p.Gly24Cys
ENST00000645020.1:n.2089G>T
ENST00000645285.1:c.70G>T	ENSP00000495058.1:p.Gly24Cys
ENST00000645331.1:n.1165G>T
ENST00000645620.1:c.70G>T	ENSP00000493657.1:p.Gly24Cys
ENST00000646777.1:n.975G>T
ENST00000647016.1:n.1279G>T
ENST00000647152.1:c.70G>T	ENSP00000495893.1:p.Gly24Cys
ENST00000647209.1:c.*668G>T	ENSP00000495558.1:n.*668G>T
ENST00000647346.1:n.1819G>T
ENST00000299427.10:c.799G>T	ENSP00000299427.6:p.Gly267Cys
ENST00000436873.6:c.451-245G>T	ENSP00000398136.2:n.451-245G>T
ENST00000524788.1:n.499G>T
ENST00000528807.1:n.349G>T
ENST00000533371.5:c.70G>T	ENSP00000437066.1:p.Gly24Cys
ENST00000611494.4:c.799G>T	ENSP00000484546.1:p.Gly267Cys
NM_000391.3:c.799G>T	NP_000382.3:p.Gly267Cys
NM_000391.4:c.799G>T MANE Select	NP_000382.3:p.Gly267Cys