Canonical Allele Identifier: CA379474626

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6637710A>G (hg19) ; chr11:g.6616479A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616479A>G , CM000673.2:g.6616479A>G	GRCh38
NC_000011.9:g.6637710A>G , CM000673.1:g.6637710A>G	GRCh37
NC_000011.8:g.6594286A>G	NCBI36
NG_008653.1:g.7983T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.797T>C	ENSP00000507321.1:p.Phe266Ser
ENST00000299427.12:c.911T>C MANE Select	ENSP00000299427.6:p.Phe304Ser
ENST00000436873.7:c.313-405T>C
ENST00000530040.2:n.504T>C
ENST00000533371.6:c.182T>C	ENSP00000437066.1:p.Phe61Ser
ENST00000642892.1:c.182T>C	ENSP00000494165.1:p.Phe61Ser
ENST00000643342.1:c.1T>C
ENST00000643439.1:c.*651T>C	ENSP00000495849.1:n.*651T>C
ENST00000643479.1:n.1097T>C
ENST00000643516.1:c.420T>C
ENST00000644218.1:c.886+182T>C	ENSP00000493574.1:n.886+182T>C
ENST00000644683.1:c.*364T>C	ENSP00000494085.1:n.*364T>C
ENST00000644810.1:c.632T>C	ENSP00000495895.1:p.Phe211Ser
ENST00000644831.1:n.1087T>C
ENST00000644933.1:c.182T>C	ENSP00000496133.1:p.Phe61Ser
ENST00000645285.1:c.157+182T>C	ENSP00000495058.1:n.157+182T>C
ENST00000645331.1:n.1434T>C
ENST00000645620.1:c.182T>C	ENSP00000493657.1:p.Phe61Ser
ENST00000646691.1:n.4T>C
ENST00000646777.1:n.1244T>C
ENST00000647016.1:n.1391T>C
ENST00000647152.1:c.182T>C	ENSP00000495893.1:p.Phe61Ser
ENST00000647209.1:c.*780T>C	ENSP00000495558.1:n.*780T>C
ENST00000647346.1:n.1931T>C
ENST00000299427.10:c.911T>C	ENSP00000299427.6:p.Phe304Ser
ENST00000436873.6:c.475T>C	ENSP00000398136.2:p.Ser159Pro
ENST00000533371.5:c.182T>C	ENSP00000437066.1:p.Phe61Ser
ENST00000611494.4:c.911T>C	ENSP00000484546.1:p.Phe304Ser
NM_000391.3:c.911T>C	NP_000382.3:p.Phe304Ser
NM_000391.4:c.911T>C MANE Select	NP_000382.3:p.Phe304Ser