Canonical Allele Identifier: CA1950237157

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616690T= , CM000673.2:g.6616690T=	GRCh38
NC_000011.9:g.6637921T= , CM000673.1:g.6637921T=	GRCh37
NC_000011.8:g.6594497T=	NCBI36
NG_008653.1:g.7772A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.743A=	ENSP00000507321.1:p.Asn248=
ENST00000299427.12:c.857A= MANE Select	ENSP00000299427.6:p.Asn286=
ENST00000436873.7:c.312+611A=
ENST00000524788.2:n.2016A=
ENST00000524903.2:n.2132A=
ENST00000528807.2:n.513A=
ENST00000530040.2:n.480-187A=
ENST00000533371.6:c.128A=	ENSP00000437066.1:p.Asn43=
ENST00000642892.1:c.128A=	ENSP00000494165.1:p.Asn43=
ENST00000643439.1:c.*597A=	ENSP00000495849.1:n.*597A=
ENST00000643479.1:n.886A=
ENST00000643516.1:c.396-187A=
ENST00000644151.1:n.2296A=
ENST00000644218.1:c.857A=	ENSP00000493574.1:p.Asn286=
ENST00000644683.1:c.*310A=	ENSP00000494085.1:n.*310A=
ENST00000644810.1:c.578A=	ENSP00000495895.1:p.Asn193=
ENST00000644831.1:n.1033A=
ENST00000644933.1:c.128A=	ENSP00000496133.1:p.Asn43=
ENST00000645020.1:n.2147A=
ENST00000645285.1:c.128A=	ENSP00000495058.1:p.Asn43=
ENST00000645331.1:n.1223A=
ENST00000645620.1:c.128A=	ENSP00000493657.1:p.Asn43=
ENST00000646777.1:n.1033A=
ENST00000647016.1:n.1337A=
ENST00000647152.1:c.128A=	ENSP00000495893.1:p.Asn43=
ENST00000647209.1:c.*726A=	ENSP00000495558.1:n.*726A=
ENST00000647346.1:n.1877A=
ENST00000299427.10:c.857A=	ENSP00000299427.6:p.Asn286=
ENST00000436873.6:c.451-187A=	ENSP00000398136.2:n.451-187A=
ENST00000528807.1:n.407A=
ENST00000533371.5:c.128A=	ENSP00000437066.1:p.Asn43=
ENST00000611494.4:c.857A=	ENSP00000484546.1:p.Asn286=
NM_000391.3:c.857A=	NP_000382.3:p.Asn286=
NM_000391.4:c.857A= MANE Select	NP_000382.3:p.Asn286=