Canonical Allele Identifier: CA217323206

Gene: TPP1

Linked Data

• dbSNP Id: rs910877083
• gnomAD v4: 11-6616898-G-A
• MyVariant Identifiers: chr11:g.6638129G>A (hg19) ; chr11:g.6616898G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616898G>A , CM000673.2:g.6616898G>A	GRCh38
NC_000011.9:g.6638129G>A , CM000673.1:g.6638129G>A	GRCh37
NC_000011.8:g.6594705G>A	NCBI36
NG_008653.1:g.7564C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.574-39C>T	ENSP00000507321.1:n.574-39C>T
ENST00000299427.12:c.688-39C>T MANE Select	ENSP00000299427.6:n.688-39C>T
ENST00000436873.7:c.312+403C>T
ENST00000524788.2:n.1847-39C>T
ENST00000524903.2:n.1963-39C>T
ENST00000528807.2:n.344-39C>T
ENST00000530040.2:n.480-395C>T
ENST00000533371.6:c.-42-39C>T	ENSP00000437066.1:n.-42-39C>T
ENST00000642892.1:c.-42-39C>T	ENSP00000494165.1:n.-42-39C>T
ENST00000643439.1:c.*428-39C>T	ENSP00000495849.1:n.*428-39C>T
ENST00000643479.1:n.717-39C>T
ENST00000643516.1:c.396-395C>T
ENST00000644151.1:n.2127-39C>T
ENST00000644218.1:c.688-39C>T	ENSP00000493574.1:n.688-39C>T
ENST00000644683.1:c.*141-39C>T	ENSP00000494085.1:n.*141-39C>T
ENST00000644810.1:c.409-39C>T	ENSP00000495895.1:n.409-39C>T
ENST00000644831.1:n.864-39C>T
ENST00000644933.1:c.-42-39C>T	ENSP00000496133.1:n.-42-39C>T
ENST00000645020.1:n.1939C>T
ENST00000645285.1:c.-42-39C>T	ENSP00000495058.1:n.-42-39C>T
ENST00000645331.1:n.1054-39C>T
ENST00000645620.1:c.-42-39C>T	ENSP00000493657.1:n.-42-39C>T
ENST00000646777.1:n.864-39C>T
ENST00000647016.1:n.1168-39C>T
ENST00000647152.1:c.-42-39C>T	ENSP00000495893.1:n.-42-39C>T
ENST00000647209.1:c.*557-39C>T	ENSP00000495558.1:n.*557-39C>T
ENST00000647346.1:n.1708-39C>T
ENST00000299427.10:c.688-39C>T	ENSP00000299427.6:n.688-39C>T
ENST00000436873.6:c.451-395C>T	ENSP00000398136.2:n.451-395C>T
ENST00000524788.1:n.388-39C>T
ENST00000528807.1:n.238-39C>T
ENST00000533371.5:c.-42-39C>T	ENSP00000437066.1:n.-42-39C>T
ENST00000611494.4:c.688-39C>T	ENSP00000484546.1:n.688-39C>T
NM_000391.3:c.688-39C>T	NP_000382.3:n.688-39C>T
NM_000391.4:c.688-39C>T MANE Select	NP_000382.3:n.688-39C>T