Canonical Allele Identifier: CA1950234616

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615484A= , CM000673.2:g.6615484A=	GRCh38
NC_000011.9:g.6636715A= , CM000673.1:g.6636715A=	GRCh37
NC_000011.8:g.6593291A=	NCBI36
NG_008653.1:g.8978T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1110T=	ENSP00000507321.1:p.Ser370=
ENST00000299427.12:c.1224T= MANE Select	ENSP00000299427.6:p.Ser408=
ENST00000436873.7:c.461T=
ENST00000524924.2:n.344T=
ENST00000533371.6:c.495T=	ENSP00000437066.1:p.Ser165=
ENST00000642892.1:c.495T=	ENSP00000494165.1:p.Ser165=
ENST00000643342.1:c.297T=
ENST00000643439.1:c.*964T=	ENSP00000495849.1:n.*964T=
ENST00000643479.1:n.1410T=
ENST00000643516.1:c.733T=
ENST00000644218.1:c.1035T=	ENSP00000493574.1:p.Ser345=
ENST00000644683.1:c.*677T=	ENSP00000494085.1:n.*677T=
ENST00000644810.1:c.945T=	ENSP00000495895.1:p.Ser315=
ENST00000644831.1:n.1400T=
ENST00000644933.1:c.*90T=	ENSP00000496133.1:n.*90T=
ENST00000645285.1:c.*90T=	ENSP00000495058.1:n.*90T=
ENST00000645331.1:n.2429T=
ENST00000645620.1:c.495T=	ENSP00000493657.1:p.Ser165=
ENST00000646691.1:n.999T=
ENST00000646777.1:n.1557T=
ENST00000647016.1:n.1704T=
ENST00000647152.1:c.495T=	ENSP00000495893.1:p.Ser165=
ENST00000647209.1:c.*1093T=	ENSP00000495558.1:n.*1093T=
ENST00000647346.1:n.2244T=
ENST00000299427.10:c.1224T=	ENSP00000299427.6:p.Ser408=
ENST00000524924.1:n.179T=
ENST00000532191.1:n.277T=
ENST00000533371.5:c.495T=	ENSP00000437066.1:p.Ser165=
ENST00000611494.4:c.1224T=	ENSP00000484546.1:p.Ser408=
NM_000391.3:c.1224T=	NP_000382.3:p.Ser408=
NM_000391.4:c.1224T= MANE Select	NP_000382.3:p.Ser408=