Canonical Allele Identifier: CA379472087

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6635853C>G (hg19) ; chr11:g.6614622C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614622C>G , CM000673.2:g.6614622C>G	GRCh38
NC_000011.9:g.6635853C>G , CM000673.1:g.6635853C>G	GRCh37
NC_000011.8:g.6592429C>G	NCBI36
NG_008653.1:g.9840G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1502G>C	ENSP00000507321.1:p.Gly501Ala
ENST00000299427.12:c.1616G>C MANE Select	ENSP00000299427.6:p.Gly539Ala
ENST00000524611.2:n.655G>C
ENST00000524924.2:n.736G>C
ENST00000533371.6:c.887G>C	ENSP00000437066.1:p.Gly296Ala
ENST00000642892.1:c.887G>C	ENSP00000494165.1:p.Gly296Ala
ENST00000643342.1:c.689G>C
ENST00000643439.1:c.*1356G>C	ENSP00000495849.1:n.*1356G>C
ENST00000643479.1:n.1802G>C
ENST00000643516.1:c.1125G>C
ENST00000644218.1:c.1427G>C	ENSP00000493574.1:p.Gly476Ala
ENST00000644683.1:c.*1069G>C	ENSP00000494085.1:n.*1069G>C
ENST00000644810.1:c.1337G>C	ENSP00000495895.1:p.Gly446Ala
ENST00000644831.1:n.1792G>C
ENST00000644933.1:c.*482G>C	ENSP00000496133.1:n.*482G>C
ENST00000645285.1:c.*482G>C	ENSP00000495058.1:n.*482G>C
ENST00000645331.1:n.2821G>C
ENST00000645620.1:c.887G>C	ENSP00000493657.1:p.Gly296Ala
ENST00000646691.1:n.1503G>C
ENST00000646777.1:n.1949G>C
ENST00000647016.1:n.2096G>C
ENST00000647152.1:c.887G>C	ENSP00000495893.1:p.Gly296Ala
ENST00000647209.1:c.*1485G>C	ENSP00000495558.1:n.*1485G>C
ENST00000647346.1:n.2636G>C
ENST00000299427.10:c.1616G>C	ENSP00000299427.6:p.Gly539Ala
ENST00000533371.5:c.887G>C	ENSP00000437066.1:p.Gly296Ala
ENST00000611494.4:c.1616G>C	ENSP00000484546.1:p.Gly539Ala
NM_000391.3:c.1616G>C	NP_000382.3:p.Gly539Ala
NM_000391.4:c.1616G>C MANE Select	NP_000382.3:p.Gly539Ala