Canonical Allele Identifier: CA1950234607

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615483C= , CM000673.2:g.6615483C=	GRCh38
NC_000011.9:g.6636714C= , CM000673.1:g.6636714C=	GRCh37
NC_000011.8:g.6593290C=	NCBI36
NG_008653.1:g.8979G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1111G=	ENSP00000507321.1:p.Gly371=
ENST00000299427.12:c.1225G= MANE Select	ENSP00000299427.6:p.Gly409=
ENST00000436873.7:c.462G=
ENST00000524924.2:n.345G=
ENST00000533371.6:c.496G=	ENSP00000437066.1:p.Gly166=
ENST00000642892.1:c.496G=	ENSP00000494165.1:p.Gly166=
ENST00000643342.1:c.298G=
ENST00000643439.1:c.*965G=	ENSP00000495849.1:n.*965G=
ENST00000643479.1:n.1411G=
ENST00000643516.1:c.734G=
ENST00000644218.1:c.1036G=	ENSP00000493574.1:p.Gly346=
ENST00000644683.1:c.*678G=	ENSP00000494085.1:n.*678G=
ENST00000644810.1:c.946G=	ENSP00000495895.1:p.Gly316=
ENST00000644831.1:n.1401G=
ENST00000644933.1:c.*91G=	ENSP00000496133.1:n.*91G=
ENST00000645285.1:c.*91G=	ENSP00000495058.1:n.*91G=
ENST00000645331.1:n.2430G=
ENST00000645620.1:c.496G=	ENSP00000493657.1:p.Gly166=
ENST00000646691.1:n.1000G=
ENST00000646777.1:n.1558G=
ENST00000647016.1:n.1705G=
ENST00000647152.1:c.496G=	ENSP00000495893.1:p.Gly166=
ENST00000647209.1:c.*1094G=	ENSP00000495558.1:n.*1094G=
ENST00000647346.1:n.2245G=
ENST00000299427.10:c.1225G=	ENSP00000299427.6:p.Gly409=
ENST00000524924.1:n.180G=
ENST00000532191.1:n.278G=
ENST00000533371.5:c.496G=	ENSP00000437066.1:p.Gly166=
ENST00000611494.4:c.1225G=	ENSP00000484546.1:p.Gly409=
NM_000391.3:c.1225G=	NP_000382.3:p.Gly409=
NM_000391.4:c.1225G= MANE Select	NP_000382.3:p.Gly409=