Canonical Allele Identifier: CA1950233873

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615184A= , CM000673.2:g.6615184A=	GRCh38
NC_000011.9:g.6636415A= , CM000673.1:g.6636415A=	GRCh37
NC_000011.8:g.6592991A=	NCBI36
NG_008653.1:g.9278T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.1298T=	ENSP00000507321.1:p.Val433=
ENST00000299427.12:c.1412T= MANE Select	ENSP00000299427.6:p.Val471=
ENST00000524611.2:n.272T=
ENST00000524924.2:n.532T=
ENST00000533371.6:c.683T=	ENSP00000437066.1:p.Val228=
ENST00000642892.1:c.683T=	ENSP00000494165.1:p.Val228=
ENST00000643342.1:c.485T=
ENST00000643439.1:c.*1152T=	ENSP00000495849.1:n.*1152T=
ENST00000643479.1:n.1598T=
ENST00000643516.1:c.921T=
ENST00000644218.1:c.1223T=	ENSP00000493574.1:p.Val408=
ENST00000644683.1:c.*865T=	ENSP00000494085.1:n.*865T=
ENST00000644810.1:c.1133T=	ENSP00000495895.1:p.Val378=
ENST00000644831.1:n.1588T=
ENST00000644933.1:c.*278T=	ENSP00000496133.1:n.*278T=
ENST00000645285.1:c.*278T=	ENSP00000495058.1:n.*278T=
ENST00000645331.1:n.2617T=
ENST00000645620.1:c.683T=	ENSP00000493657.1:p.Val228=
ENST00000646691.1:n.1299T=
ENST00000646777.1:n.1745T=
ENST00000647016.1:n.1892T=
ENST00000647152.1:c.683T=	ENSP00000495893.1:p.Val228=
ENST00000647209.1:c.*1281T=	ENSP00000495558.1:n.*1281T=
ENST00000647346.1:n.2432T=
ENST00000299427.10:c.1412T=	ENSP00000299427.6:p.Val471=
ENST00000524611.1:n.290T=
ENST00000533371.5:c.683T=	ENSP00000437066.1:p.Val228=
ENST00000611494.4:c.1412T=	ENSP00000484546.1:p.Val471=
NM_000391.3:c.1412T=	NP_000382.3:p.Val471=
NM_000391.4:c.1412T= MANE Select	NP_000382.3:p.Val471=