Canonical Allele Identifier: CA319225

Gene: TPP1

Linked Data

• ClinVar Variation Id: 207600
• ClinVar RCV Id: RCV000384515 ; RCV000725967
• dbSNP Id: rs200138397
• ExAC: 11:6637982 G / A
• gnomAD v2: 11-6637982-G-A
• gnomAD v3: 11-6616751-G-A
• gnomAD v4: 11-6616751-G-A
• MyVariant Identifiers: chr11:g.6637982G>A (hg19) ; chr11:g.6616751G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616751G>A , CM000673.2:g.6616751G>A	GRCh38
NC_000011.9:g.6637982G>A , CM000673.1:g.6637982G>A	GRCh37
NC_000011.8:g.6594558G>A	NCBI36
NG_008653.1:g.7711C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.682C>T	ENSP00000507321.1:p.Arg228Trp
ENST00000299427.12:c.796C>T MANE Select	ENSP00000299427.6:p.Arg266Trp
ENST00000436873.7:c.312+550C>T
ENST00000524788.2:n.1955C>T
ENST00000524903.2:n.2071C>T
ENST00000528807.2:n.452C>T
ENST00000530040.2:n.480-248C>T
ENST00000533371.6:c.67C>T	ENSP00000437066.1:p.Arg23Trp
ENST00000642892.1:c.67C>T	ENSP00000494165.1:p.Arg23Trp
ENST00000643439.1:c.*536C>T	ENSP00000495849.1:n.*536C>T
ENST00000643479.1:n.825C>T
ENST00000643516.1:c.396-248C>T
ENST00000644151.1:n.2235C>T
ENST00000644218.1:c.796C>T	ENSP00000493574.1:p.Arg266Trp
ENST00000644683.1:c.*249C>T	ENSP00000494085.1:n.*249C>T
ENST00000644810.1:c.517C>T	ENSP00000495895.1:p.Arg173Trp
ENST00000644831.1:n.972C>T
ENST00000644933.1:c.67C>T	ENSP00000496133.1:p.Arg23Trp
ENST00000645020.1:n.2086C>T
ENST00000645285.1:c.67C>T	ENSP00000495058.1:p.Arg23Trp
ENST00000645331.1:n.1162C>T
ENST00000645620.1:c.67C>T	ENSP00000493657.1:p.Arg23Trp
ENST00000646777.1:n.972C>T
ENST00000647016.1:n.1276C>T
ENST00000647152.1:c.67C>T	ENSP00000495893.1:p.Arg23Trp
ENST00000647209.1:c.*665C>T	ENSP00000495558.1:n.*665C>T
ENST00000647346.1:n.1816C>T
ENST00000299427.10:c.796C>T	ENSP00000299427.6:p.Arg266Trp
ENST00000436873.6:c.451-248C>T	ENSP00000398136.2:n.451-248C>T
ENST00000524788.1:n.496C>T
ENST00000528807.1:n.346C>T
ENST00000533371.5:c.67C>T	ENSP00000437066.1:p.Arg23Trp
ENST00000611494.4:c.796C>T	ENSP00000484546.1:p.Arg266Trp
NM_000391.3:c.796C>T	NP_000382.3:p.Arg266Trp
NM_000391.4:c.796C>T MANE Select	NP_000382.3:p.Arg266Trp