Canonical Allele Identifier: CA1950237723

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616994T= , CM000673.2:g.6616994T=	GRCh38
NC_000011.9:g.6638225T= , CM000673.1:g.6638225T=	GRCh37
NC_000011.8:g.6594801T=	NCBI36
NG_008653.1:g.7468A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.554A=	ENSP00000507321.1:p.Asn185=
ENST00000299427.12:c.668A= MANE Select	ENSP00000299427.6:p.Asn223=
ENST00000436873.7:c.312+307A=
ENST00000524788.2:n.1827A=
ENST00000524903.2:n.1943A=
ENST00000528807.2:n.324A=
ENST00000530040.2:n.479+365A=
ENST00000533371.6:c.-62A=	ENSP00000437066.1:n.-62A=
ENST00000534644.6:n.616A=
ENST00000642892.1:c.-62A=	ENSP00000494165.1:n.-62A=
ENST00000643439.1:c.*408A=	ENSP00000495849.1:n.*408A=
ENST00000643479.1:n.697A=
ENST00000643516.1:c.395+307A=
ENST00000644151.1:n.2107A=
ENST00000644218.1:c.668A=	ENSP00000493574.1:p.Asn223=
ENST00000644683.1:c.*121A=	ENSP00000494085.1:n.*121A=
ENST00000644810.1:c.389A=	ENSP00000495895.1:p.Asn130=
ENST00000644831.1:n.844A=
ENST00000644933.1:c.-62A=	ENSP00000496133.1:n.-62A=
ENST00000645020.1:n.1843A=
ENST00000645285.1:c.-62A=	ENSP00000495058.1:n.-62A=
ENST00000645331.1:n.1034A=
ENST00000645620.1:c.-62A=	ENSP00000493657.1:n.-62A=
ENST00000646777.1:n.844A=
ENST00000647016.1:n.1148A=
ENST00000647152.1:c.-62A=	ENSP00000495893.1:n.-62A=
ENST00000647209.1:c.*537A=	ENSP00000495558.1:n.*537A=
ENST00000647346.1:n.1688A=
ENST00000299427.10:c.668A=	ENSP00000299427.6:p.Asn223=
ENST00000428886.6:n.837A=
ENST00000436873.6:c.450+365A=	ENSP00000398136.2:n.450+365A=
ENST00000524788.1:n.368A=
ENST00000528571.5:c.*408A=	ENSP00000434647.1:n.*408A=
ENST00000528807.1:n.218A=
ENST00000533371.5:c.-62A=	ENSP00000437066.1:n.-62A=
ENST00000611494.4:c.668A=	ENSP00000484546.1:p.Asn223=
NM_000391.3:c.668A=	NP_000382.3:p.Asn223=
NM_000391.4:c.668A= MANE Select	NP_000382.3:p.Asn223=