Canonical Allele Identifier: CA217320689

Gene: TPP1

Linked Data

• dbSNP Id: rs913373160
• gnomAD v4: 11-6614483-A-G
• MyVariant Identifiers: chr11:g.6635714A>G (hg19) ; chr11:g.6614483A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614483A>G , CM000673.2:g.6614483A>G	GRCh38
NC_000011.9:g.6635714A>G , CM000673.1:g.6635714A>G	GRCh37
NC_000011.8:g.6592290A>G	NCBI36
NG_008653.1:g.9979T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.*63T>C	ENSP00000507321.1:n.*63T>C
ENST00000299427.12:c.*63T>C MANE Select	ENSP00000299427.6:n.*63T>C
ENST00000524611.2:n.794T>C
ENST00000533371.6:c.*63T>C	ENSP00000437066.1:n.*63T>C
ENST00000642892.1:c.*63T>C	ENSP00000494165.1:n.*63T>C
ENST00000643342.1:c.828T>C
ENST00000643439.1:c.*1495T>C	ENSP00000495849.1:n.*1495T>C
ENST00000643479.1:n.1941T>C
ENST00000643516.1:c.1264T>C
ENST00000644218.1:c.*63T>C	ENSP00000493574.1:n.*63T>C
ENST00000644683.1:c.*1208T>C	ENSP00000494085.1:n.*1208T>C
ENST00000644810.1:c.*63T>C	ENSP00000495895.1:n.*63T>C
ENST00000644831.1:n.1931T>C
ENST00000644933.1:c.*621T>C	ENSP00000496133.1:n.*621T>C
ENST00000645285.1:c.*621T>C	ENSP00000495058.1:n.*621T>C
ENST00000645331.1:n.2960T>C
ENST00000645620.1:c.*63T>C	ENSP00000493657.1:n.*63T>C
ENST00000646691.1:n.1642T>C
ENST00000646777.1:n.2088T>C
ENST00000647016.1:n.2235T>C
ENST00000647152.1:c.*63T>C	ENSP00000495893.1:n.*63T>C
ENST00000647209.1:c.*1624T>C	ENSP00000495558.1:n.*1624T>C
ENST00000647346.1:n.2775T>C
ENST00000299427.10:c.*63T>C	ENSP00000299427.6:n.*63T>C
ENST00000533371.5:c.*63T>C	ENSP00000437066.1:n.*63T>C
ENST00000611494.4:c.*83T>C	ENSP00000484546.1:n.*83T>C
NM_000391.3:c.*63T>C	NP_000382.3:n.*63T>C
NM_000391.4:c.*63T>C MANE Select	NP_000382.3:n.*63T>C