Canonical Allele Identifier: CA5858862

Gene: TPP1

Linked Data

• dbSNP Id: rs760831786
• ExAC: 11:6638123 C / A
• gnomAD v2: 11-6638123-C-A
• MyVariant Identifiers: chr11:g.6638123C>A (hg19) ; chr11:g.6616892C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616892C>A , CM000673.2:g.6616892C>A	GRCh38
NC_000011.9:g.6638123C>A , CM000673.1:g.6638123C>A	GRCh37
NC_000011.8:g.6594699C>A	NCBI36
NG_008653.1:g.7570G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.574-33G>T	ENSP00000507321.1:n.574-33G>T
ENST00000299427.12:c.688-33G>T MANE Select	ENSP00000299427.6:n.688-33G>T
ENST00000436873.7:c.312+409G>T
ENST00000524788.2:n.1847-33G>T
ENST00000524903.2:n.1963-33G>T
ENST00000528807.2:n.344-33G>T
ENST00000530040.2:n.480-389G>T
ENST00000533371.6:c.-42-33G>T	ENSP00000437066.1:n.-42-33G>T
ENST00000642892.1:c.-42-33G>T	ENSP00000494165.1:n.-42-33G>T
ENST00000643439.1:c.*428-33G>T	ENSP00000495849.1:n.*428-33G>T
ENST00000643479.1:n.717-33G>T
ENST00000643516.1:c.396-389G>T
ENST00000644151.1:n.2127-33G>T
ENST00000644218.1:c.688-33G>T	ENSP00000493574.1:n.688-33G>T
ENST00000644683.1:c.*141-33G>T	ENSP00000494085.1:n.*141-33G>T
ENST00000644810.1:c.409-33G>T	ENSP00000495895.1:n.409-33G>T
ENST00000644831.1:n.864-33G>T
ENST00000644933.1:c.-42-33G>T	ENSP00000496133.1:n.-42-33G>T
ENST00000645020.1:n.1945G>T
ENST00000645285.1:c.-42-33G>T	ENSP00000495058.1:n.-42-33G>T
ENST00000645331.1:n.1054-33G>T
ENST00000645620.1:c.-42-33G>T	ENSP00000493657.1:n.-42-33G>T
ENST00000646777.1:n.864-33G>T
ENST00000647016.1:n.1168-33G>T
ENST00000647152.1:c.-42-33G>T	ENSP00000495893.1:n.-42-33G>T
ENST00000647209.1:c.*557-33G>T	ENSP00000495558.1:n.*557-33G>T
ENST00000647346.1:n.1708-33G>T
ENST00000299427.10:c.688-33G>T	ENSP00000299427.6:n.688-33G>T
ENST00000436873.6:c.451-389G>T	ENSP00000398136.2:n.451-389G>T
ENST00000524788.1:n.388-33G>T
ENST00000528807.1:n.238-33G>T
ENST00000533371.5:c.-42-33G>T	ENSP00000437066.1:n.-42-33G>T
ENST00000611494.4:c.688-33G>T	ENSP00000484546.1:n.688-33G>T
NM_000391.3:c.688-33G>T	NP_000382.3:n.688-33G>T
NM_000391.4:c.688-33G>T MANE Select	NP_000382.3:n.688-33G>T