Canonical Allele Identifier: CA2574741360

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617219_6617222dup , CM000673.2:g.6617219_6617222dup	GRCh38
NC_000011.9:g.6638450_6638453dup , CM000673.1:g.6638450_6638453dup	GRCh37
NC_000011.8:g.6595026_6595029dup	NCBI36
NG_008653.1:g.7243_7246dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.395-66_395-63dup	ENSP00000507321.1:n.395-66_395-63dup
ENST00000299427.12:c.509-66_509-63dup MANE Select	ENSP00000299427.6:n.509-66_509-63dup
ENST00000428886.7:n.678_681dup
ENST00000436873.7:c.312+82_312+85dup
ENST00000524788.2:n.1602_1605dup
ENST00000524903.2:n.1718_1721dup
ENST00000528571.6:c.*330_*333dup	ENSP00000434647.1:n.*330_*333dup
ENST00000528807.2:n.165-66_165-63dup
ENST00000530040.2:n.479+140_479+143dup
ENST00000533371.6:c.-221-66_-221-63dup	ENSP00000437066.1:n.-221-66_-221-63dup
ENST00000534644.6:n.457-66_457-63dup
ENST00000642892.1:c.-221-66_-221-63dup	ENSP00000494165.1:n.-221-66_-221-63dup
ENST00000643439.1:c.*249-66_*249-63dup	ENSP00000495849.1:n.*249-66_*249-63dup
ENST00000643479.1:n.538-66_538-63dup
ENST00000643516.1:c.395+82_395+85dup
ENST00000644151.1:n.1882_1885dup
ENST00000644218.1:c.509-66_509-63dup	ENSP00000493574.1:n.509-66_509-63dup
ENST00000644683.1:c.451-66_451-63dup	ENSP00000494085.1:n.451-66_451-63dup
ENST00000644810.1:c.230-66_230-63dup	ENSP00000495895.1:n.230-66_230-63dup
ENST00000644831.1:n.619_622dup
ENST00000644933.1:c.-221-66_-221-63dup	ENSP00000496133.1:n.-221-66_-221-63dup
ENST00000645020.1:n.1618_1621dup
ENST00000645285.1:c.-221-66_-221-63dup	ENSP00000495058.1:n.-221-66_-221-63dup
ENST00000645331.1:n.809_812dup
ENST00000645620.1:c.-221-66_-221-63dup	ENSP00000493657.1:n.-221-66_-221-63dup
ENST00000646777.1:n.619_622dup
ENST00000647016.1:n.923_926dup
ENST00000647152.1:c.-221-66_-221-63dup	ENSP00000495893.1:n.-221-66_-221-63dup
ENST00000647209.1:c.*378-66_*378-63dup	ENSP00000495558.1:n.*378-66_*378-63dup
ENST00000647346.1:n.1529-66_1529-63dup
ENST00000299427.10:c.509-66_509-63dup	ENSP00000299427.6:n.509-66_509-63dup
ENST00000428886.6:n.612_615dup
ENST00000436873.6:c.450+140_450+143dup	ENSP00000398136.2:n.450+140_450+143dup
ENST00000524788.1:n.143_146dup
ENST00000528571.5:c.*249-66_*249-63dup	ENSP00000434647.1:n.*249-66_*249-63dup
ENST00000533371.5:c.-221-66_-221-63dup	ENSP00000437066.1:n.-221-66_-221-63dup
ENST00000534644.5:n.494-66_494-63dup
ENST00000611494.4:c.509-66_509-63dup	ENSP00000484546.1:n.509-66_509-63dup
NM_000391.3:c.509-66_509-63dup	NP_000382.3:n.509-66_509-63dup
NM_000391.4:c.509-66_509-63dup MANE Select	NP_000382.3:n.509-66_509-63dup