Canonical Allele Identifier: CA217322404

Gene: TPP1

Linked Data

• dbSNP Id: rs1021545730
• gnomAD v4: 11-6616274-C-T
• MyVariant Identifiers: chr11:g.6637505C>T (hg19) ; chr11:g.6616274C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616274C>T , CM000673.2:g.6616274C>T	GRCh38
NC_000011.9:g.6637505C>T , CM000673.1:g.6637505C>T	GRCh37
NC_000011.8:g.6594081C>T	NCBI36
NG_008653.1:g.8188G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.961+41G>A	ENSP00000507321.1:n.961+41G>A
ENST00000299427.12:c.1075+41G>A MANE Select	ENSP00000299427.6:n.1075+41G>A
ENST00000436873.7:c.313-200G>A
ENST00000533371.6:c.346+41G>A	ENSP00000437066.1:n.346+41G>A
ENST00000642892.1:c.346+41G>A	ENSP00000494165.1:n.346+41G>A
ENST00000643342.1:c.165+41G>A
ENST00000643439.1:c.*815+41G>A	ENSP00000495849.1:n.*815+41G>A
ENST00000643479.1:n.1261+41G>A
ENST00000643516.1:c.584+41G>A
ENST00000644218.1:c.887-200G>A	ENSP00000493574.1:n.887-200G>A
ENST00000644683.1:c.*528+41G>A	ENSP00000494085.1:n.*528+41G>A
ENST00000644810.1:c.796+41G>A	ENSP00000495895.1:n.796+41G>A
ENST00000644831.1:n.1251+41G>A
ENST00000644933.1:c.346+41G>A	ENSP00000496133.1:n.346+41G>A
ENST00000645285.1:c.158-200G>A	ENSP00000495058.1:n.158-200G>A
ENST00000645331.1:n.1639G>A
ENST00000645620.1:c.346+41G>A	ENSP00000493657.1:n.346+41G>A
ENST00000646691.1:n.209G>A
ENST00000646777.1:n.1408+41G>A
ENST00000647016.1:n.1555+41G>A
ENST00000647152.1:c.346+41G>A	ENSP00000495893.1:n.346+41G>A
ENST00000647209.1:c.*944+41G>A	ENSP00000495558.1:n.*944+41G>A
ENST00000647346.1:n.2095+41G>A
ENST00000299427.10:c.1075+41G>A	ENSP00000299427.6:n.1075+41G>A
ENST00000533371.5:c.346+41G>A	ENSP00000437066.1:n.346+41G>A
ENST00000611494.4:c.1075+41G>A	ENSP00000484546.1:n.1075+41G>A
NM_000391.3:c.1075+41G>A	NP_000382.3:n.1075+41G>A
NM_000391.4:c.1075+41G>A MANE Select	NP_000382.3:n.1075+41G>A