Canonical Allele Identifier: CA2697548400

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615761C>T , CM000673.2:g.6615761C>T	GRCh38
NC_000011.9:g.6636992C>T , CM000673.1:g.6636992C>T	GRCh37
NC_000011.8:g.6593568C>T	NCBI36
NG_008653.1:g.8701G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000391.4:c.1146-199G>A MANE Select	NP_000382.3:n.1146-199G>A
ENST00000299427.12:c.1146-199G>A MANE Select	ENSP00000299427.6:n.1146-199G>A
NM_000391.3:c.1146-199G>A	NP_000382.3:n.1146-199G>A
ENST00000299427.10:c.1146-199G>A	ENSP00000299427.6:n.1146-199G>A
ENST00000436873.7:c.383-199G>A
ENST00000524924.1:n.101-199G>A
ENST00000524924.2:n.266-199G>A
ENST00000533371.5:c.417-199G>A	ENSP00000437066.1:n.417-199G>A
ENST00000533371.6:c.417-199G>A	ENSP00000437066.1:n.417-199G>A
ENST00000611494.4:c.1146-199G>A	ENSP00000484546.1:n.1146-199G>A
ENST00000642892.1:c.417-199G>A	ENSP00000494165.1:n.417-199G>A
ENST00000643342.1:c.236-216G>A
ENST00000643439.1:c.*886-199G>A	ENSP00000495849.1:n.*886-199G>A
ENST00000643479.1:n.1332-199G>A
ENST00000643516.1:c.655-199G>A
ENST00000644218.1:c.957-199G>A	ENSP00000493574.1:n.957-199G>A
ENST00000644683.1:c.*599-199G>A	ENSP00000494085.1:n.*599-199G>A
ENST00000644810.1:c.867-199G>A	ENSP00000495895.1:n.867-199G>A
ENST00000644831.1:n.1322-199G>A
ENST00000644933.1:c.*11+4G>A	ENSP00000496133.1:n.*11+4G>A
ENST00000645285.1:c.*11+4G>A	ENSP00000495058.1:n.*11+4G>A
ENST00000645331.1:n.2152G>A
ENST00000645620.1:c.417-199G>A	ENSP00000493657.1:n.417-199G>A
ENST00000646691.1:n.722G>A
ENST00000646777.1:n.1479-199G>A
ENST00000647016.1:n.1626-199G>A
ENST00000647152.1:c.417-199G>A	ENSP00000495893.1:n.417-199G>A
ENST00000647209.1:c.*1015-199G>A	ENSP00000495558.1:n.*1015-199G>A
ENST00000647346.1:n.2166-199G>A
ENST00000682424.1:c.1032-199G>A	ENSP00000507321.1:n.1032-199G>A