Canonical Allele Identifier: CA379475023

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6637963T>G (hg19) ; chr11:g.6616732T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616732T>G , CM000673.2:g.6616732T>G	GRCh38
NC_000011.9:g.6637963T>G , CM000673.1:g.6637963T>G	GRCh37
NC_000011.8:g.6594539T>G	NCBI36
NG_008653.1:g.7730A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.701A>C	ENSP00000507321.1:p.Glu234Ala
ENST00000299427.12:c.815A>C MANE Select	ENSP00000299427.6:p.Glu272Ala
ENST00000436873.7:c.312+569A>C
ENST00000524788.2:n.1974A>C
ENST00000524903.2:n.2090A>C
ENST00000528807.2:n.471A>C
ENST00000530040.2:n.480-229A>C
ENST00000533371.6:c.86A>C	ENSP00000437066.1:p.Glu29Ala
ENST00000642892.1:c.86A>C	ENSP00000494165.1:p.Glu29Ala
ENST00000643439.1:c.*555A>C	ENSP00000495849.1:n.*555A>C
ENST00000643479.1:n.844A>C
ENST00000643516.1:c.396-229A>C
ENST00000644151.1:n.2254A>C
ENST00000644218.1:c.815A>C	ENSP00000493574.1:p.Glu272Ala
ENST00000644683.1:c.*268A>C	ENSP00000494085.1:n.*268A>C
ENST00000644810.1:c.536A>C	ENSP00000495895.1:p.Glu179Ala
ENST00000644831.1:n.991A>C
ENST00000644933.1:c.86A>C	ENSP00000496133.1:p.Glu29Ala
ENST00000645020.1:n.2105A>C
ENST00000645285.1:c.86A>C	ENSP00000495058.1:p.Glu29Ala
ENST00000645331.1:n.1181A>C
ENST00000645620.1:c.86A>C	ENSP00000493657.1:p.Glu29Ala
ENST00000646777.1:n.991A>C
ENST00000647016.1:n.1295A>C
ENST00000647152.1:c.86A>C	ENSP00000495893.1:p.Glu29Ala
ENST00000647209.1:c.*684A>C	ENSP00000495558.1:n.*684A>C
ENST00000647346.1:n.1835A>C
ENST00000299427.10:c.815A>C	ENSP00000299427.6:p.Glu272Ala
ENST00000436873.6:c.451-229A>C	ENSP00000398136.2:n.451-229A>C
ENST00000524788.1:n.515A>C
ENST00000528807.1:n.365A>C
ENST00000533371.5:c.86A>C	ENSP00000437066.1:p.Glu29Ala
ENST00000611494.4:c.815A>C	ENSP00000484546.1:p.Glu272Ala
NM_000391.3:c.815A>C	NP_000382.3:p.Glu272Ala
NM_000391.4:c.815A>C MANE Select	NP_000382.3:p.Glu272Ala