Canonical Allele Identifier: CA2790314292

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616535_6616541del , CM000673.2:g.6616535_6616541del	GRCh38
NC_000011.9:g.6637766_6637772del , CM000673.1:g.6637766_6637772del	GRCh37
NC_000011.8:g.6594342_6594348del	NCBI36
NG_008653.1:g.7921_7927del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.773-38_773-32del	ENSP00000507321.1:n.773-38_773-32del
ENST00000299427.12:c.887-38_887-32del MANE Select	ENSP00000299427.6:n.887-38_887-32del
ENST00000436873.7:c.313-467_313-461del
ENST00000524903.2:n.2281_2287del
ENST00000530040.2:n.480-38_480-32del
ENST00000533371.6:c.158-38_158-32del	ENSP00000437066.1:n.158-38_158-32del
ENST00000642892.1:c.158-38_158-32del	ENSP00000494165.1:n.158-38_158-32del
ENST00000643439.1:c.*627-38_*627-32del	ENSP00000495849.1:n.*627-38_*627-32del
ENST00000643479.1:n.1035_1041del
ENST00000643516.1:c.396-38_396-32del
ENST00000644218.1:c.886+120_886+126del	ENSP00000493574.1:n.886+120_886+126del
ENST00000644683.1:c.*340-38_*340-32del	ENSP00000494085.1:n.*340-38_*340-32del
ENST00000644810.1:c.608-38_608-32del	ENSP00000495895.1:n.608-38_608-32del
ENST00000644831.1:n.1063-38_1063-32del
ENST00000644933.1:c.158-38_158-32del	ENSP00000496133.1:n.158-38_158-32del
ENST00000645285.1:c.157+120_157+126del	ENSP00000495058.1:n.157+120_157+126del
ENST00000645331.1:n.1372_1378del
ENST00000645620.1:c.158-38_158-32del	ENSP00000493657.1:n.158-38_158-32del
ENST00000646777.1:n.1182_1188del
ENST00000647016.1:n.1367-38_1367-32del
ENST00000647152.1:c.158-38_158-32del	ENSP00000495893.1:n.158-38_158-32del
ENST00000647209.1:c.*756-38_*756-32del	ENSP00000495558.1:n.*756-38_*756-32del
ENST00000647346.1:n.1907-38_1907-32del
ENST00000299427.10:c.887-38_887-32del	ENSP00000299427.6:n.887-38_887-32del
ENST00000436873.6:c.451-38_451-32del	ENSP00000398136.2:n.451-38_451-32del
ENST00000528807.1:n.556_562del
ENST00000533371.5:c.158-38_158-32del	ENSP00000437066.1:n.158-38_158-32del
ENST00000611494.4:c.887-38_887-32del	ENSP00000484546.1:n.887-38_887-32del
NM_000391.3:c.887-38_887-32del	NP_000382.3:n.887-38_887-32del
NM_000391.4:c.887-38_887-32del MANE Select	NP_000382.3:n.887-38_887-32del