Canonical Allele Identifier: CA1950238244

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617174_6617177delinsTGAG , CM000673.2:g.6617174_6617177delinsTGAG	GRCh38
NC_000011.9:g.6638405_6638408delinsTGAG , CM000673.1:g.6638405_6638408delinsTGAG	GRCh37
NC_000011.8:g.6594981_6594984delinsTGAG	NCBI36
NG_008653.1:g.7285_7288delinsCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.395-24_395-21delinsCTCA	ENSP00000507321.1:n.395-24_395-21delinsCTCA
ENST00000299427.12:c.509-24_509-21delinsCTCA MANE Select	ENSP00000299427.6:n.509-24_509-21delinsCTCA
ENST00000428886.7:n.720_723delinsCTCA
ENST00000436873.7:c.312+124_312+127delinsCTCA
ENST00000524788.2:n.1644_1647delinsCTCA
ENST00000524903.2:n.1760_1763delinsCTCA
ENST00000528807.2:n.165-24_165-21delinsCTCA
ENST00000530040.2:n.479+182_479+185delinsCTCA
ENST00000533371.6:c.-221-24_-221-21delinsCTCA	ENSP00000437066.1:n.-221-24_-221-21delinsCTCA
ENST00000534644.6:n.457-24_457-21delinsCTCA
ENST00000642892.1:c.-221-24_-221-21delinsCTCA	ENSP00000494165.1:n.-221-24_-221-21delinsCTCA
ENST00000643439.1:c.*249-24_*249-21delinsCTCA	ENSP00000495849.1:n.*249-24_*249-21delinsCTCA
ENST00000643479.1:n.538-24_538-21delinsCTCA
ENST00000643516.1:c.395+124_395+127delinsCTCA
ENST00000644151.1:n.1924_1927delinsCTCA
ENST00000644218.1:c.509-24_509-21delinsCTCA	ENSP00000493574.1:n.509-24_509-21delinsCTCA
ENST00000644683.1:c.451-24_451-21delinsCTCA	ENSP00000494085.1:n.451-24_451-21delinsCTCA
ENST00000644810.1:c.230-24_230-21delinsCTCA	ENSP00000495895.1:n.230-24_230-21delinsCTCA
ENST00000644831.1:n.661_664delinsCTCA
ENST00000644933.1:c.-221-24_-221-21delinsCTCA	ENSP00000496133.1:n.-221-24_-221-21delinsCTCA
ENST00000645020.1:n.1660_1663delinsCTCA
ENST00000645285.1:c.-221-24_-221-21delinsCTCA	ENSP00000495058.1:n.-221-24_-221-21delinsCTCA
ENST00000645331.1:n.851_854delinsCTCA
ENST00000645620.1:c.-221-24_-221-21delinsCTCA	ENSP00000493657.1:n.-221-24_-221-21delinsCTCA
ENST00000646777.1:n.661_664delinsCTCA
ENST00000647016.1:n.965_968delinsCTCA
ENST00000647152.1:c.-221-24_-221-21delinsCTCA	ENSP00000495893.1:n.-221-24_-221-21delinsCTCA
ENST00000647209.1:c.*378-24_*378-21delinsCTCA	ENSP00000495558.1:n.*378-24_*378-21delinsCTCA
ENST00000647346.1:n.1529-24_1529-21delinsCTCA
ENST00000299427.10:c.509-24_509-21delinsCTCA	ENSP00000299427.6:n.509-24_509-21delinsCTCA
ENST00000428886.6:n.654_657delinsCTCA
ENST00000436873.6:c.450+182_450+185delinsCTCA	ENSP00000398136.2:n.450+182_450+185delinsCTCA
ENST00000524788.1:n.185_188delinsCTCA
ENST00000528571.5:c.*249-24_*249-21delinsCTCA	ENSP00000434647.1:n.*249-24_*249-21delinsCTCA
ENST00000528807.1:n.35_38delinsCTCA
ENST00000533371.5:c.-221-24_-221-21delinsCTCA	ENSP00000437066.1:n.-221-24_-221-21delinsCTCA
ENST00000534644.5:n.494-24_494-21delinsCTCA
ENST00000611494.4:c.509-24_509-21delinsCTCA	ENSP00000484546.1:n.509-24_509-21delinsCTCA
NM_000391.3:c.509-24_509-21delinsCTCA	NP_000382.3:n.509-24_509-21delinsCTCA
NM_000391.4:c.509-24_509-21delinsCTCA MANE Select	NP_000382.3:n.509-24_509-21delinsCTCA