Canonical Allele Identifier: CA1950235739

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616068C= , CM000673.2:g.6616068C=	GRCh38
NC_000011.9:g.6637299C= , CM000673.1:g.6637299C=	GRCh37
NC_000011.8:g.6593875C=	NCBI36
NG_008653.1:g.8394G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.968G=	ENSP00000507321.1:p.Ser323=
ENST00000299427.12:c.1082G= MANE Select	ENSP00000299427.6:p.Ser361=
ENST00000436873.7:c.319G=
ENST00000524924.2:n.202G=
ENST00000533371.6:c.353G=	ENSP00000437066.1:p.Ser118=
ENST00000642892.1:c.353G=	ENSP00000494165.1:p.Ser118=
ENST00000643342.1:c.172G=
ENST00000643439.1:c.*822G=	ENSP00000495849.1:n.*822G=
ENST00000643479.1:n.1268G=
ENST00000643516.1:c.591G=
ENST00000644218.1:c.893G=	ENSP00000493574.1:p.Ser298=
ENST00000644683.1:c.*535G=	ENSP00000494085.1:n.*535G=
ENST00000644810.1:c.803G=	ENSP00000495895.1:p.Ser268=
ENST00000644831.1:n.1258G=
ENST00000644933.1:c.353G=	ENSP00000496133.1:p.Ser118=
ENST00000645285.1:c.164G=	ENSP00000495058.1:p.Ser55=
ENST00000645331.1:n.1845G=
ENST00000645620.1:c.353G=	ENSP00000493657.1:p.Ser118=
ENST00000646691.1:n.415G=
ENST00000646777.1:n.1415G=
ENST00000647016.1:n.1562G=
ENST00000647152.1:c.353G=	ENSP00000495893.1:p.Ser118=
ENST00000647209.1:c.*951G=	ENSP00000495558.1:n.*951G=
ENST00000647346.1:n.2102G=
ENST00000299427.10:c.1082G=	ENSP00000299427.6:p.Ser361=
ENST00000524924.1:n.37G=
ENST00000533371.5:c.353G=	ENSP00000437066.1:p.Ser118=
ENST00000611494.4:c.1082G=	ENSP00000484546.1:p.Ser361=
NM_000391.3:c.1082G=	NP_000382.3:p.Ser361=
NM_000391.4:c.1082G= MANE Select	NP_000382.3:p.Ser361=