Canonical Allele Identifier: CA2790314342

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617204_6617206del , CM000673.2:g.6617204_6617206del	GRCh38
NC_000011.9:g.6638435_6638437del , CM000673.1:g.6638435_6638437del	GRCh37
NC_000011.8:g.6595011_6595013del	NCBI36
NG_008653.1:g.7256_7258del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.395-53_395-51del	ENSP00000507321.1:n.395-53_395-51del
ENST00000299427.12:c.509-53_509-51del MANE Select	ENSP00000299427.6:n.509-53_509-51del
ENST00000428886.7:n.691_693del
ENST00000436873.7:c.312+95_312+97del
ENST00000524788.2:n.1615_1617del
ENST00000524903.2:n.1731_1733del
ENST00000528807.2:n.165-53_165-51del
ENST00000530040.2:n.479+153_479+155del
ENST00000533371.6:c.-221-53_-221-51del	ENSP00000437066.1:n.-221-53_-221-51del
ENST00000534644.6:n.457-53_457-51del
ENST00000642892.1:c.-221-53_-221-51del	ENSP00000494165.1:n.-221-53_-221-51del
ENST00000643439.1:c.*249-53_*249-51del	ENSP00000495849.1:n.*249-53_*249-51del
ENST00000643479.1:n.538-53_538-51del
ENST00000643516.1:c.395+95_395+97del
ENST00000644151.1:n.1895_1897del
ENST00000644218.1:c.509-53_509-51del	ENSP00000493574.1:n.509-53_509-51del
ENST00000644683.1:c.451-53_451-51del	ENSP00000494085.1:n.451-53_451-51del
ENST00000644810.1:c.230-53_230-51del	ENSP00000495895.1:n.230-53_230-51del
ENST00000644831.1:n.632_634del
ENST00000644933.1:c.-221-53_-221-51del	ENSP00000496133.1:n.-221-53_-221-51del
ENST00000645020.1:n.1631_1633del
ENST00000645285.1:c.-221-53_-221-51del	ENSP00000495058.1:n.-221-53_-221-51del
ENST00000645331.1:n.822_824del
ENST00000645620.1:c.-221-53_-221-51del	ENSP00000493657.1:n.-221-53_-221-51del
ENST00000646777.1:n.632_634del
ENST00000647016.1:n.936_938del
ENST00000647152.1:c.-221-53_-221-51del	ENSP00000495893.1:n.-221-53_-221-51del
ENST00000647209.1:c.*378-53_*378-51del	ENSP00000495558.1:n.*378-53_*378-51del
ENST00000647346.1:n.1529-53_1529-51del
ENST00000299427.10:c.509-53_509-51del	ENSP00000299427.6:n.509-53_509-51del
ENST00000428886.6:n.625_627del
ENST00000436873.6:c.450+153_450+155del	ENSP00000398136.2:n.450+153_450+155del
ENST00000524788.1:n.156_158del
ENST00000528571.5:c.*249-53_*249-51del	ENSP00000434647.1:n.*249-53_*249-51del
ENST00000528807.1:n.6_8del
ENST00000533371.5:c.-221-53_-221-51del	ENSP00000437066.1:n.-221-53_-221-51del
ENST00000534644.5:n.494-53_494-51del
ENST00000611494.4:c.509-53_509-51del	ENSP00000484546.1:n.509-53_509-51del
NM_000391.3:c.509-53_509-51del	NP_000382.3:n.509-53_509-51del
NM_000391.4:c.509-53_509-51del MANE Select	NP_000382.3:n.509-53_509-51del