Canonical Allele Identifier: CA1950235939

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616146G= , CM000673.2:g.6616146G=	GRCh38
NC_000011.9:g.6637377G= , CM000673.1:g.6637377G=	GRCh37
NC_000011.8:g.6593953G=	NCBI36
NG_008653.1:g.8316C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.962-72C=	ENSP00000507321.1:n.962-72C=
ENST00000299427.12:c.1076-72C= MANE Select	ENSP00000299427.6:n.1076-72C=
ENST00000436873.7:c.313-72C=
ENST00000524924.2:n.124C=
ENST00000533371.6:c.347-72C=	ENSP00000437066.1:n.347-72C=
ENST00000642892.1:c.347-72C=	ENSP00000494165.1:n.347-72C=
ENST00000643342.1:c.166-72C=
ENST00000643439.1:c.*816-72C=	ENSP00000495849.1:n.*816-72C=
ENST00000643479.1:n.1262-72C=
ENST00000643516.1:c.585-72C=
ENST00000644218.1:c.887-72C=	ENSP00000493574.1:n.887-72C=
ENST00000644683.1:c.*529-72C=	ENSP00000494085.1:n.*529-72C=
ENST00000644810.1:c.797-72C=	ENSP00000495895.1:n.797-72C=
ENST00000644831.1:n.1252-72C=
ENST00000644933.1:c.347-72C=	ENSP00000496133.1:n.347-72C=
ENST00000645285.1:c.158-72C=	ENSP00000495058.1:n.158-72C=
ENST00000645331.1:n.1767C=
ENST00000645620.1:c.347-72C=	ENSP00000493657.1:n.347-72C=
ENST00000646691.1:n.337C=
ENST00000646777.1:n.1409-72C=
ENST00000647016.1:n.1556-72C=
ENST00000647152.1:c.347-72C=	ENSP00000495893.1:n.347-72C=
ENST00000647209.1:c.*945-72C=	ENSP00000495558.1:n.*945-72C=
ENST00000647346.1:n.2096-72C=
ENST00000299427.10:c.1076-72C=	ENSP00000299427.6:n.1076-72C=
ENST00000533371.5:c.347-72C=	ENSP00000437066.1:n.347-72C=
ENST00000611494.4:c.1076-72C=	ENSP00000484546.1:n.1076-72C=
NM_000391.3:c.1076-72C=	NP_000382.3:n.1076-72C=
NM_000391.4:c.1076-72C= MANE Select	NP_000382.3:n.1076-72C=