Canonical Allele Identifier: CA379472879

Gene: TPP1

Linked Data

• gnomAD v4: 11-6615453-G-T
• MyVariant Identifiers: chr11:g.6636684G>T (hg19) ; chr11:g.6615453G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615453G>T , CM000673.2:g.6615453G>T	GRCh38
NC_000011.9:g.6636684G>T , CM000673.1:g.6636684G>T	GRCh37
NC_000011.8:g.6593260G>T	NCBI36
NG_008653.1:g.9009C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1141C>A	ENSP00000507321.1:p.Pro381Thr
ENST00000299427.12:c.1255C>A MANE Select	ENSP00000299427.6:p.Pro419Thr
ENST00000436873.7:c.492C>A
ENST00000524611.2:n.3C>A
ENST00000524924.2:n.375C>A
ENST00000533371.6:c.526C>A	ENSP00000437066.1:p.Pro176Thr
ENST00000642892.1:c.526C>A	ENSP00000494165.1:p.Pro176Thr
ENST00000643342.1:c.328C>A
ENST00000643439.1:c.*995C>A	ENSP00000495849.1:n.*995C>A
ENST00000643479.1:n.1441C>A
ENST00000643516.1:c.764C>A
ENST00000644218.1:c.1066C>A	ENSP00000493574.1:p.Pro356Thr
ENST00000644683.1:c.*708C>A	ENSP00000494085.1:n.*708C>A
ENST00000644810.1:c.976C>A	ENSP00000495895.1:p.Pro326Thr
ENST00000644831.1:n.1431C>A
ENST00000644933.1:c.*121C>A	ENSP00000496133.1:n.*121C>A
ENST00000645285.1:c.*121C>A	ENSP00000495058.1:n.*121C>A
ENST00000645331.1:n.2460C>A
ENST00000645620.1:c.526C>A	ENSP00000493657.1:p.Pro176Thr
ENST00000646691.1:n.1030C>A
ENST00000646777.1:n.1588C>A
ENST00000647016.1:n.1735C>A
ENST00000647152.1:c.526C>A	ENSP00000495893.1:p.Pro176Thr
ENST00000647209.1:c.*1124C>A	ENSP00000495558.1:n.*1124C>A
ENST00000647346.1:n.2275C>A
ENST00000299427.10:c.1255C>A	ENSP00000299427.6:p.Pro419Thr
ENST00000524611.1:n.21C>A
ENST00000524924.1:n.210C>A
ENST00000532191.1:n.308C>A
ENST00000533371.5:c.526C>A	ENSP00000437066.1:p.Pro176Thr
ENST00000611494.4:c.1255C>A	ENSP00000484546.1:p.Pro419Thr
NM_000391.3:c.1255C>A	NP_000382.3:p.Pro419Thr
NM_000391.4:c.1255C>A MANE Select	NP_000382.3:p.Pro419Thr