Canonical Allele Identifier: CA379475029

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6637966A>C (hg19) ; chr11:g.6616735A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616735A>C , CM000673.2:g.6616735A>C	GRCh38
NC_000011.9:g.6637966A>C , CM000673.1:g.6637966A>C	GRCh37
NC_000011.8:g.6594542A>C	NCBI36
NG_008653.1:g.7727T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.698T>G	ENSP00000507321.1:p.Ile233Ser
ENST00000299427.12:c.812T>G MANE Select	ENSP00000299427.6:p.Ile271Ser
ENST00000436873.7:c.312+566T>G
ENST00000524788.2:n.1971T>G
ENST00000524903.2:n.2087T>G
ENST00000528807.2:n.468T>G
ENST00000530040.2:n.480-232T>G
ENST00000533371.6:c.83T>G	ENSP00000437066.1:p.Ile28Ser
ENST00000642892.1:c.83T>G	ENSP00000494165.1:p.Ile28Ser
ENST00000643439.1:c.*552T>G	ENSP00000495849.1:n.*552T>G
ENST00000643479.1:n.841T>G
ENST00000643516.1:c.396-232T>G
ENST00000644151.1:n.2251T>G
ENST00000644218.1:c.812T>G	ENSP00000493574.1:p.Ile271Ser
ENST00000644683.1:c.*265T>G	ENSP00000494085.1:n.*265T>G
ENST00000644810.1:c.533T>G	ENSP00000495895.1:p.Ile178Ser
ENST00000644831.1:n.988T>G
ENST00000644933.1:c.83T>G	ENSP00000496133.1:p.Ile28Ser
ENST00000645020.1:n.2102T>G
ENST00000645285.1:c.83T>G	ENSP00000495058.1:p.Ile28Ser
ENST00000645331.1:n.1178T>G
ENST00000645620.1:c.83T>G	ENSP00000493657.1:p.Ile28Ser
ENST00000646777.1:n.988T>G
ENST00000647016.1:n.1292T>G
ENST00000647152.1:c.83T>G	ENSP00000495893.1:p.Ile28Ser
ENST00000647209.1:c.*681T>G	ENSP00000495558.1:n.*681T>G
ENST00000647346.1:n.1832T>G
ENST00000299427.10:c.812T>G	ENSP00000299427.6:p.Ile271Ser
ENST00000436873.6:c.451-232T>G	ENSP00000398136.2:n.451-232T>G
ENST00000524788.1:n.512T>G
ENST00000528807.1:n.362T>G
ENST00000533371.5:c.83T>G	ENSP00000437066.1:p.Ile28Ser
ENST00000611494.4:c.812T>G	ENSP00000484546.1:p.Ile271Ser
NM_000391.3:c.812T>G	NP_000382.3:p.Ile271Ser
NM_000391.4:c.812T>G MANE Select	NP_000382.3:p.Ile271Ser