Canonical Allele Identifier: CA1950215361

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617734G= , CM000673.2:g.6617734G=	GRCh38
NC_000011.9:g.6638965G= , CM000673.1:g.6638965G=	GRCh37
NC_000011.8:g.6595541G=	NCBI36
NG_008653.1:g.6728C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.158C=	ENSP00000507321.1:p.Pro53=
ENST00000299427.12:c.272C= MANE Select	ENSP00000299427.6:p.Pro91=
ENST00000428886.7:n.360C=
ENST00000436873.7:c.76C=
ENST00000524788.2:n.1284C=
ENST00000524903.2:n.1400C=
ENST00000528571.6:c.*12C=	ENSP00000434647.1:n.*12C=
ENST00000530040.2:n.301C=
ENST00000533371.6:c.-458C=	ENSP00000437066.1:n.-458C=
ENST00000534644.6:n.273C=
ENST00000642892.1:c.-405C=	ENSP00000494165.1:n.-405C=
ENST00000643439.1:c.*12C=	ENSP00000495849.1:n.*12C=
ENST00000643479.1:n.301C=
ENST00000643516.1:c.159C=
ENST00000644151.1:n.1564C=
ENST00000644218.1:c.272C=	ENSP00000493574.1:p.Pro91=
ENST00000644683.1:c.272C=	ENSP00000494085.1:p.Pro91=
ENST00000644810.1:c.230-581C=	ENSP00000495895.1:n.230-581C=
ENST00000644831.1:n.301C=
ENST00000644933.1:c.-458C=	ENSP00000496133.1:n.-458C=
ENST00000645020.1:n.1300C=
ENST00000645285.1:c.-458C=	ENSP00000495058.1:n.-458C=
ENST00000645331.1:n.294C=
ENST00000645620.1:c.-400C=	ENSP00000493657.1:n.-400C=
ENST00000646777.1:n.301C=
ENST00000647016.1:n.605C=
ENST00000647152.1:c.-458C=	ENSP00000495893.1:n.-458C=
ENST00000647209.1:c.*141C=	ENSP00000495558.1:n.*141C=
ENST00000647346.1:n.1292C=
ENST00000299427.10:c.272C=	ENSP00000299427.6:p.Pro91=
ENST00000428886.6:n.294C=
ENST00000436873.6:c.272C=	ENSP00000398136.2:p.Pro91=
ENST00000528571.5:c.*12C=	ENSP00000434647.1:n.*12C=
ENST00000530040.1:n.384C=
ENST00000533371.5:c.-458C=	ENSP00000437066.1:n.-458C=
ENST00000534644.5:n.257C=
ENST00000611494.4:c.272C=	ENSP00000484546.1:p.Pro91=
NM_000391.3:c.272C=	NP_000382.3:p.Pro91=
NM_000391.4:c.272C= MANE Select	NP_000382.3:p.Pro91=