Canonical Allele Identifier: CA2790314304

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616554_6616564del , CM000673.2:g.6616554_6616564del	GRCh38
NC_000011.9:g.6637785_6637795del , CM000673.1:g.6637785_6637795del	GRCh37
NC_000011.8:g.6594361_6594371del	NCBI36
NG_008653.1:g.7899_7909del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.773-60_773-50del	ENSP00000507321.1:n.773-60_773-50del
ENST00000299427.12:c.887-60_887-50del MANE Select	ENSP00000299427.6:n.887-60_887-50del
ENST00000436873.7:c.313-489_313-479del
ENST00000524903.2:n.2259_2269del
ENST00000528807.2:n.640_650del
ENST00000530040.2:n.480-60_480-50del
ENST00000533371.6:c.158-60_158-50del	ENSP00000437066.1:n.158-60_158-50del
ENST00000642892.1:c.158-60_158-50del	ENSP00000494165.1:n.158-60_158-50del
ENST00000643439.1:c.*627-60_*627-50del	ENSP00000495849.1:n.*627-60_*627-50del
ENST00000643479.1:n.1013_1023del
ENST00000643516.1:c.396-60_396-50del
ENST00000644218.1:c.886+98_886+108del	ENSP00000493574.1:n.886+98_886+108del
ENST00000644683.1:c.*340-60_*340-50del	ENSP00000494085.1:n.*340-60_*340-50del
ENST00000644810.1:c.608-60_608-50del	ENSP00000495895.1:n.608-60_608-50del
ENST00000644831.1:n.1063-60_1063-50del
ENST00000644933.1:c.158-60_158-50del	ENSP00000496133.1:n.158-60_158-50del
ENST00000645020.1:n.2274_2284del
ENST00000645285.1:c.157+98_157+108del	ENSP00000495058.1:n.157+98_157+108del
ENST00000645331.1:n.1350_1360del
ENST00000645620.1:c.158-60_158-50del	ENSP00000493657.1:n.158-60_158-50del
ENST00000646777.1:n.1160_1170del
ENST00000647016.1:n.1367-60_1367-50del
ENST00000647152.1:c.158-60_158-50del	ENSP00000495893.1:n.158-60_158-50del
ENST00000647209.1:c.*756-60_*756-50del	ENSP00000495558.1:n.*756-60_*756-50del
ENST00000647346.1:n.1907-60_1907-50del
ENST00000299427.10:c.887-60_887-50del	ENSP00000299427.6:n.887-60_887-50del
ENST00000436873.6:c.451-60_451-50del	ENSP00000398136.2:n.451-60_451-50del
ENST00000528807.1:n.534_544del
ENST00000533371.5:c.158-60_158-50del	ENSP00000437066.1:n.158-60_158-50del
ENST00000611494.4:c.887-60_887-50del	ENSP00000484546.1:n.887-60_887-50del
NM_000391.3:c.887-60_887-50del	NP_000382.3:n.887-60_887-50del
NM_000391.4:c.887-60_887-50del MANE Select	NP_000382.3:n.887-60_887-50del