Canonical Allele Identifier: CA1950238065

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617128_6617129delinsTG , CM000673.2:g.6617128_6617129delinsTG	GRCh38
NC_000011.9:g.6638359_6638360delinsTG , CM000673.1:g.6638359_6638360delinsTG	GRCh37
NC_000011.8:g.6594935_6594936delinsTG	NCBI36
NG_008653.1:g.7333_7334delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.419_420delinsCA	ENSP00000507321.1:p.Pro140=
ENST00000299427.12:c.533_534delinsCA MANE Select	ENSP00000299427.6:p.Pro178=
ENST00000428886.7:n.768_769delinsCA
ENST00000436873.7:c.312+172_312+173delinsCA
ENST00000524788.2:n.1692_1693delinsCA
ENST00000524903.2:n.1808_1809delinsCA
ENST00000528807.2:n.189_190delinsCA
ENST00000530040.2:n.479+230_479+231delinsCA
ENST00000533371.6:c.-197_-196delinsCA	ENSP00000437066.1:n.-197_-196delinsCA
ENST00000534644.6:n.481_482delinsCA
ENST00000642892.1:c.-197_-196delinsCA	ENSP00000494165.1:n.-197_-196delinsCA
ENST00000643439.1:c.*273_*274delinsCA	ENSP00000495849.1:n.*273_*274delinsCA
ENST00000643479.1:n.562_563delinsCA
ENST00000643516.1:c.395+172_395+173delinsCA
ENST00000644151.1:n.1972_1973delinsCA
ENST00000644218.1:c.533_534delinsCA	ENSP00000493574.1:p.Pro178=
ENST00000644683.1:c.475_476delinsCA	ENSP00000494085.1:p.Gln159=
ENST00000644810.1:c.254_255delinsCA	ENSP00000495895.1:p.Pro85=
ENST00000644831.1:n.709_710delinsCA
ENST00000644933.1:c.-197_-196delinsCA	ENSP00000496133.1:n.-197_-196delinsCA
ENST00000645020.1:n.1708_1709delinsCA
ENST00000645285.1:c.-197_-196delinsCA	ENSP00000495058.1:n.-197_-196delinsCA
ENST00000645331.1:n.899_900delinsCA
ENST00000645620.1:c.-197_-196delinsCA	ENSP00000493657.1:n.-197_-196delinsCA
ENST00000646777.1:n.709_710delinsCA
ENST00000647016.1:n.1013_1014delinsCA
ENST00000647152.1:c.-197_-196delinsCA	ENSP00000495893.1:n.-197_-196delinsCA
ENST00000647209.1:c.*402_*403delinsCA	ENSP00000495558.1:n.*402_*403delinsCA
ENST00000647346.1:n.1553_1554delinsCA
ENST00000299427.10:c.533_534delinsCA	ENSP00000299427.6:p.Pro178=
ENST00000428886.6:n.702_703delinsCA
ENST00000436873.6:c.450+230_450+231delinsCA	ENSP00000398136.2:n.450+230_450+231delinsCA
ENST00000524788.1:n.233_234delinsCA
ENST00000528571.5:c.*273_*274delinsCA	ENSP00000434647.1:n.*273_*274delinsCA
ENST00000528807.1:n.83_84delinsCA
ENST00000533371.5:c.-197_-196delinsCA	ENSP00000437066.1:n.-197_-196delinsCA
ENST00000534644.5:n.518_519delinsCA
ENST00000611494.4:c.533_534delinsCA	ENSP00000484546.1:p.Pro178=
NM_000391.3:c.533_534delinsCA	NP_000382.3:p.Pro178=
NM_000391.4:c.533_534delinsCA MANE Select	NP_000382.3:p.Pro178=