Canonical Allele Identifier: CA2790314340

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617197_6617198insACAG , CM000673.2:g.6617197_6617198insACAG	GRCh38
NC_000011.9:g.6638428_6638429insACAG , CM000673.1:g.6638428_6638429insACAG	GRCh37
NC_000011.8:g.6595004_6595005insACAG	NCBI36
NG_008653.1:g.7264_7265insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.395-45_395-44insCTGT	ENSP00000507321.1:n.395-45_395-44insCTGT
ENST00000299427.12:c.509-45_509-44insCTGT MANE Select	ENSP00000299427.6:n.509-45_509-44insCTGT
ENST00000428886.7:n.699_700insCTGT
ENST00000436873.7:c.312+103_312+104insCTGT
ENST00000524788.2:n.1623_1624insCTGT
ENST00000524903.2:n.1739_1740insCTGT
ENST00000528807.2:n.165-45_165-44insCTGT
ENST00000530040.2:n.479+161_479+162insCTGT
ENST00000533371.6:c.-221-45_-221-44insCTGT	ENSP00000437066.1:n.-221-45_-221-44insCTGT
ENST00000534644.6:n.457-45_457-44insCTGT
ENST00000642892.1:c.-221-45_-221-44insCTGT	ENSP00000494165.1:n.-221-45_-221-44insCTGT
ENST00000643439.1:c.*249-45_*249-44insCTGT	ENSP00000495849.1:n.*249-45_*249-44insCTGT
ENST00000643479.1:n.538-45_538-44insCTGT
ENST00000643516.1:c.395+103_395+104insCTGT
ENST00000644151.1:n.1903_1904insCTGT
ENST00000644218.1:c.509-45_509-44insCTGT	ENSP00000493574.1:n.509-45_509-44insCTGT
ENST00000644683.1:c.451-45_451-44insCTGT	ENSP00000494085.1:n.451-45_451-44insCTGT
ENST00000644810.1:c.230-45_230-44insCTGT	ENSP00000495895.1:n.230-45_230-44insCTGT
ENST00000644831.1:n.640_641insCTGT
ENST00000644933.1:c.-221-45_-221-44insCTGT	ENSP00000496133.1:n.-221-45_-221-44insCTGT
ENST00000645020.1:n.1639_1640insCTGT
ENST00000645285.1:c.-221-45_-221-44insCTGT	ENSP00000495058.1:n.-221-45_-221-44insCTGT
ENST00000645331.1:n.830_831insCTGT
ENST00000645620.1:c.-221-45_-221-44insCTGT	ENSP00000493657.1:n.-221-45_-221-44insCTGT
ENST00000646777.1:n.640_641insCTGT
ENST00000647016.1:n.944_945insCTGT
ENST00000647152.1:c.-221-45_-221-44insCTGT	ENSP00000495893.1:n.-221-45_-221-44insCTGT
ENST00000647209.1:c.*378-45_*378-44insCTGT	ENSP00000495558.1:n.*378-45_*378-44insCTGT
ENST00000647346.1:n.1529-45_1529-44insCTGT
ENST00000299427.10:c.509-45_509-44insCTGT	ENSP00000299427.6:n.509-45_509-44insCTGT
ENST00000428886.6:n.633_634insCTGT
ENST00000436873.6:c.450+161_450+162insCTGT	ENSP00000398136.2:n.450+161_450+162insCTGT
ENST00000524788.1:n.164_165insCTGT
ENST00000528571.5:c.*249-45_*249-44insCTGT	ENSP00000434647.1:n.*249-45_*249-44insCTGT
ENST00000528807.1:n.14_15insCTGT
ENST00000533371.5:c.-221-45_-221-44insCTGT	ENSP00000437066.1:n.-221-45_-221-44insCTGT
ENST00000534644.5:n.494-45_494-44insCTGT
ENST00000611494.4:c.509-45_509-44insCTGT	ENSP00000484546.1:n.509-45_509-44insCTGT
NM_000391.3:c.509-45_509-44insCTGT	NP_000382.3:n.509-45_509-44insCTGT
NM_000391.4:c.509-45_509-44insCTGT MANE Select	NP_000382.3:n.509-45_509-44insCTGT