Canonical Allele Identifier: CA379472078

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6635848C>G (hg19) ; chr11:g.6614617C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614617C>G , CM000673.2:g.6614617C>G	GRCh38
NC_000011.9:g.6635848C>G , CM000673.1:g.6635848C>G	GRCh37
NC_000011.8:g.6592424C>G	NCBI36
NG_008653.1:g.9845G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1507G>C	ENSP00000507321.1:p.Gly503Arg
ENST00000299427.12:c.1621G>C MANE Select	ENSP00000299427.6:p.Gly541Arg
ENST00000524611.2:n.660G>C
ENST00000524924.2:n.741G>C
ENST00000533371.6:c.892G>C	ENSP00000437066.1:p.Gly298Arg
ENST00000642892.1:c.892G>C	ENSP00000494165.1:p.Gly298Arg
ENST00000643342.1:c.694G>C
ENST00000643439.1:c.*1361G>C	ENSP00000495849.1:n.*1361G>C
ENST00000643479.1:n.1807G>C
ENST00000643516.1:c.1130G>C
ENST00000644218.1:c.1432G>C	ENSP00000493574.1:p.Gly478Arg
ENST00000644683.1:c.*1074G>C	ENSP00000494085.1:n.*1074G>C
ENST00000644810.1:c.1342G>C	ENSP00000495895.1:p.Gly448Arg
ENST00000644831.1:n.1797G>C
ENST00000644933.1:c.*487G>C	ENSP00000496133.1:n.*487G>C
ENST00000645285.1:c.*487G>C	ENSP00000495058.1:n.*487G>C
ENST00000645331.1:n.2826G>C
ENST00000645620.1:c.892G>C	ENSP00000493657.1:p.Gly298Arg
ENST00000646691.1:n.1508G>C
ENST00000646777.1:n.1954G>C
ENST00000647016.1:n.2101G>C
ENST00000647152.1:c.892G>C	ENSP00000495893.1:p.Gly298Arg
ENST00000647209.1:c.*1490G>C	ENSP00000495558.1:n.*1490G>C
ENST00000647346.1:n.2641G>C
ENST00000299427.10:c.1621G>C	ENSP00000299427.6:p.Gly541Arg
ENST00000533371.5:c.892G>C	ENSP00000437066.1:p.Gly298Arg
ENST00000611494.4:c.1621G>C	ENSP00000484546.1:p.Gly541Arg
NM_000391.3:c.1621G>C	NP_000382.3:p.Gly541Arg
NM_000391.4:c.1621G>C MANE Select	NP_000382.3:p.Gly541Arg