Canonical Allele Identifier: CA379472653

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6636472A>G (hg19) ; chr11:g.6615241A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615241A>G , CM000673.2:g.6615241A>G	GRCh38
NC_000011.9:g.6636472A>G , CM000673.1:g.6636472A>G	GRCh37
NC_000011.8:g.6593048A>G	NCBI36
NG_008653.1:g.9221T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1241T>C	ENSP00000507321.1:p.Val414Ala
ENST00000299427.12:c.1355T>C MANE Select	ENSP00000299427.6:p.Val452Ala
ENST00000524611.2:n.215T>C
ENST00000524924.2:n.475T>C
ENST00000533371.6:c.626T>C	ENSP00000437066.1:p.Val209Ala
ENST00000642892.1:c.626T>C	ENSP00000494165.1:p.Val209Ala
ENST00000643342.1:c.428T>C
ENST00000643439.1:c.*1095T>C	ENSP00000495849.1:n.*1095T>C
ENST00000643479.1:n.1541T>C
ENST00000643516.1:c.864T>C
ENST00000644218.1:c.1166T>C	ENSP00000493574.1:p.Val389Ala
ENST00000644683.1:c.*808T>C	ENSP00000494085.1:n.*808T>C
ENST00000644810.1:c.1076T>C	ENSP00000495895.1:p.Val359Ala
ENST00000644831.1:n.1531T>C
ENST00000644933.1:c.*221T>C	ENSP00000496133.1:n.*221T>C
ENST00000645285.1:c.*221T>C	ENSP00000495058.1:n.*221T>C
ENST00000645331.1:n.2560T>C
ENST00000645620.1:c.626T>C	ENSP00000493657.1:p.Val209Ala
ENST00000646691.1:n.1242T>C
ENST00000646777.1:n.1688T>C
ENST00000647016.1:n.1835T>C
ENST00000647152.1:c.626T>C	ENSP00000495893.1:p.Val209Ala
ENST00000647209.1:c.*1224T>C	ENSP00000495558.1:n.*1224T>C
ENST00000647346.1:n.2375T>C
ENST00000299427.10:c.1355T>C	ENSP00000299427.6:p.Val452Ala
ENST00000524611.1:n.233T>C
ENST00000532191.1:n.408T>C
ENST00000533371.5:c.626T>C	ENSP00000437066.1:p.Val209Ala
ENST00000611494.4:c.1355T>C	ENSP00000484546.1:p.Val452Ala
NM_000391.3:c.1355T>C	NP_000382.3:p.Val452Ala
NM_000391.4:c.1355T>C MANE Select	NP_000382.3:p.Val452Ala