Canonical Allele Identifier: CA1950232649

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614596A= , CM000673.2:g.6614596A=	GRCh38
NC_000011.9:g.6635827A= , CM000673.1:g.6635827A=	GRCh37
NC_000011.8:g.6592403A=	NCBI36
NG_008653.1:g.9866T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1528T=	ENSP00000507321.1:p.Trp510=
ENST00000299427.12:c.1642T= MANE Select	ENSP00000299427.6:p.Trp548=
ENST00000524611.2:n.681T=
ENST00000533371.6:c.913T=	ENSP00000437066.1:p.Trp305=
ENST00000642892.1:c.913T=	ENSP00000494165.1:p.Trp305=
ENST00000643342.1:c.715T=
ENST00000643439.1:c.*1382T=	ENSP00000495849.1:n.*1382T=
ENST00000643479.1:n.1828T=
ENST00000643516.1:c.1151T=
ENST00000644218.1:c.1453T=	ENSP00000493574.1:p.Trp485=
ENST00000644683.1:c.*1095T=	ENSP00000494085.1:n.*1095T=
ENST00000644810.1:c.1363T=	ENSP00000495895.1:p.Trp455=
ENST00000644831.1:n.1818T=
ENST00000644933.1:c.*508T=	ENSP00000496133.1:n.*508T=
ENST00000645285.1:c.*508T=	ENSP00000495058.1:n.*508T=
ENST00000645331.1:n.2847T=
ENST00000645620.1:c.913T=	ENSP00000493657.1:p.Trp305=
ENST00000646691.1:n.1529T=
ENST00000646777.1:n.1975T=
ENST00000647016.1:n.2122T=
ENST00000647152.1:c.913T=	ENSP00000495893.1:p.Trp305=
ENST00000647209.1:c.*1511T=	ENSP00000495558.1:n.*1511T=
ENST00000647346.1:n.2662T=
ENST00000299427.10:c.1642T=	ENSP00000299427.6:p.Trp548=
ENST00000533371.5:c.913T=	ENSP00000437066.1:p.Trp305=
ENST00000611494.4:c.1642T=	ENSP00000484546.1:p.Trp548=
NM_000391.3:c.1642T=	NP_000382.3:p.Trp548=
NM_000391.4:c.1642T= MANE Select	NP_000382.3:p.Trp548=