Canonical Allele Identifier: CA1950236349

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616355C= , CM000673.2:g.6616355C=	GRCh38
NC_000011.9:g.6637586C= , CM000673.1:g.6637586C=	GRCh37
NC_000011.8:g.6594162C=	NCBI36
NG_008653.1:g.8107G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.921G=	ENSP00000507321.1:p.Met307=
ENST00000299427.12:c.1035G= MANE Select	ENSP00000299427.6:p.Met345=
ENST00000436873.7:c.313-281G=
ENST00000533371.6:c.306G=	ENSP00000437066.1:p.Met102=
ENST00000642892.1:c.306G=	ENSP00000494165.1:p.Met102=
ENST00000643342.1:c.125G=
ENST00000643439.1:c.*775G=	ENSP00000495849.1:n.*775G=
ENST00000643479.1:n.1221G=
ENST00000643516.1:c.544G=
ENST00000644218.1:c.887-281G=	ENSP00000493574.1:n.887-281G=
ENST00000644683.1:c.*488G=	ENSP00000494085.1:n.*488G=
ENST00000644810.1:c.756G=	ENSP00000495895.1:p.Met252=
ENST00000644831.1:n.1211G=
ENST00000644933.1:c.306G=	ENSP00000496133.1:p.Met102=
ENST00000645285.1:c.158-281G=	ENSP00000495058.1:n.158-281G=
ENST00000645331.1:n.1558G=
ENST00000645620.1:c.306G=	ENSP00000493657.1:p.Met102=
ENST00000646691.1:n.128G=
ENST00000646777.1:n.1368G=
ENST00000647016.1:n.1515G=
ENST00000647152.1:c.306G=	ENSP00000495893.1:p.Met102=
ENST00000647209.1:c.*904G=	ENSP00000495558.1:n.*904G=
ENST00000647346.1:n.2055G=
ENST00000299427.10:c.1035G=	ENSP00000299427.6:p.Met345=
ENST00000533371.5:c.306G=	ENSP00000437066.1:p.Met102=
ENST00000611494.4:c.1035G=	ENSP00000484546.1:p.Met345=
NM_000391.3:c.1035G=	NP_000382.3:p.Met345=
NM_000391.4:c.1035G= MANE Select	NP_000382.3:p.Met345=