Canonical Allele Identifier: CA379472838

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6636559T>A (hg19) ; chr11:g.6615328T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615328T>A , CM000673.2:g.6615328T>A	GRCh38
NC_000011.9:g.6636559T>A , CM000673.1:g.6636559T>A	GRCh37
NC_000011.8:g.6593135T>A	NCBI36
NG_008653.1:g.9134A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1154A>T	ENSP00000507321.1:p.Glu385Val
ENST00000299427.12:c.1268A>T MANE Select	ENSP00000299427.6:p.Glu423Val
ENST00000436873.7:c.505A>T
ENST00000524611.2:n.128A>T
ENST00000524924.2:n.388A>T
ENST00000533371.6:c.539A>T	ENSP00000437066.1:p.Glu180Val
ENST00000642892.1:c.539A>T	ENSP00000494165.1:p.Glu180Val
ENST00000643342.1:c.341A>T
ENST00000643439.1:c.*1008A>T	ENSP00000495849.1:n.*1008A>T
ENST00000643479.1:n.1454A>T
ENST00000643516.1:c.777A>T
ENST00000644218.1:c.1079A>T	ENSP00000493574.1:p.Glu360Val
ENST00000644683.1:c.*721A>T	ENSP00000494085.1:n.*721A>T
ENST00000644810.1:c.989A>T	ENSP00000495895.1:p.Glu330Val
ENST00000644831.1:n.1444A>T
ENST00000644933.1:c.*134A>T	ENSP00000496133.1:n.*134A>T
ENST00000645285.1:c.*134A>T	ENSP00000495058.1:n.*134A>T
ENST00000645331.1:n.2473A>T
ENST00000645620.1:c.539A>T	ENSP00000493657.1:p.Glu180Val
ENST00000646691.1:n.1155A>T
ENST00000646777.1:n.1601A>T
ENST00000647016.1:n.1748A>T
ENST00000647152.1:c.539A>T	ENSP00000495893.1:p.Glu180Val
ENST00000647209.1:c.*1137A>T	ENSP00000495558.1:n.*1137A>T
ENST00000647346.1:n.2288A>T
ENST00000299427.10:c.1268A>T	ENSP00000299427.6:p.Glu423Val
ENST00000524611.1:n.146A>T
ENST00000524924.1:n.223A>T
ENST00000532191.1:n.321A>T
ENST00000533371.5:c.539A>T	ENSP00000437066.1:p.Glu180Val
ENST00000611494.4:c.1268A>T	ENSP00000484546.1:p.Glu423Val
NM_000391.3:c.1268A>T	NP_000382.3:p.Glu423Val
NM_000391.4:c.1268A>T MANE Select	NP_000382.3:p.Glu423Val