Canonical Allele Identifier: CA2841969355

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616647C>A , CM000673.2:g.6616647C>A	GRCh38
NC_000011.9:g.6637878C>A , CM000673.1:g.6637878C>A	GRCh37
NC_000011.8:g.6594454C>A	NCBI36
NG_008653.1:g.7815G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.772+14G>T	ENSP00000507321.1:n.772+14G>T
ENST00000299427.12:c.886+14G>T MANE Select	ENSP00000299427.6:n.886+14G>T
ENST00000436873.7:c.313-573G>T
ENST00000524788.2:n.2059G>T
ENST00000524903.2:n.2175G>T
ENST00000528807.2:n.556G>T
ENST00000530040.2:n.480-144G>T
ENST00000533371.6:c.157+14G>T	ENSP00000437066.1:n.157+14G>T
ENST00000642892.1:c.157+14G>T	ENSP00000494165.1:n.157+14G>T
ENST00000643439.1:c.*626+14G>T	ENSP00000495849.1:n.*626+14G>T
ENST00000643479.1:n.929G>T
ENST00000643516.1:c.396-144G>T
ENST00000644218.1:c.886+14G>T	ENSP00000493574.1:n.886+14G>T
ENST00000644683.1:c.*339+14G>T	ENSP00000494085.1:n.*339+14G>T
ENST00000644810.1:c.607+14G>T	ENSP00000495895.1:n.607+14G>T
ENST00000644831.1:n.1062+14G>T
ENST00000644933.1:c.157+14G>T	ENSP00000496133.1:n.157+14G>T
ENST00000645020.1:n.2190G>T
ENST00000645285.1:c.157+14G>T	ENSP00000495058.1:n.157+14G>T
ENST00000645331.1:n.1266G>T
ENST00000645620.1:c.157+14G>T	ENSP00000493657.1:n.157+14G>T
ENST00000646777.1:n.1076G>T
ENST00000647016.1:n.1366+14G>T
ENST00000647152.1:c.157+14G>T	ENSP00000495893.1:n.157+14G>T
ENST00000647209.1:c.*755+14G>T	ENSP00000495558.1:n.*755+14G>T
ENST00000647346.1:n.1906+14G>T
ENST00000299427.10:c.886+14G>T	ENSP00000299427.6:n.886+14G>T
ENST00000436873.6:c.451-144G>T	ENSP00000398136.2:n.451-144G>T
ENST00000528807.1:n.450G>T
ENST00000533371.5:c.157+14G>T	ENSP00000437066.1:n.157+14G>T
ENST00000611494.4:c.886+14G>T	ENSP00000484546.1:n.886+14G>T
NM_000391.3:c.886+14G>T	NP_000382.3:n.886+14G>T
NM_000391.4:c.886+14G>T MANE Select	NP_000382.3:n.886+14G>T