Canonical Allele Identifier: CA1950238135

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617148C= , CM000673.2:g.6617148C=	GRCh38
NC_000011.9:g.6638379C= , CM000673.1:g.6638379C=	GRCh37
NC_000011.8:g.6594955C=	NCBI36
NG_008653.1:g.7314G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.400G=	ENSP00000507321.1:p.Gly134=
ENST00000299427.12:c.514G= MANE Select	ENSP00000299427.6:p.Gly172=
ENST00000428886.7:n.749G=
ENST00000436873.7:c.312+153G=
ENST00000524788.2:n.1673G=
ENST00000524903.2:n.1789G=
ENST00000528807.2:n.170G=
ENST00000530040.2:n.479+211G=
ENST00000533371.6:c.-216G=	ENSP00000437066.1:n.-216G=
ENST00000534644.6:n.462G=
ENST00000642892.1:c.-216G=	ENSP00000494165.1:n.-216G=
ENST00000643439.1:c.*254G=	ENSP00000495849.1:n.*254G=
ENST00000643479.1:n.543G=
ENST00000643516.1:c.395+153G=
ENST00000644151.1:n.1953G=
ENST00000644218.1:c.514G=	ENSP00000493574.1:p.Gly172=
ENST00000644683.1:c.456G=	ENSP00000494085.1:p.Gly152=
ENST00000644810.1:c.235G=	ENSP00000495895.1:p.Gly79=
ENST00000644831.1:n.690G=
ENST00000644933.1:c.-216G=	ENSP00000496133.1:n.-216G=
ENST00000645020.1:n.1689G=
ENST00000645285.1:c.-216G=	ENSP00000495058.1:n.-216G=
ENST00000645331.1:n.880G=
ENST00000645620.1:c.-216G=	ENSP00000493657.1:n.-216G=
ENST00000646777.1:n.690G=
ENST00000647016.1:n.994G=
ENST00000647152.1:c.-216G=	ENSP00000495893.1:n.-216G=
ENST00000647209.1:c.*383G=	ENSP00000495558.1:n.*383G=
ENST00000647346.1:n.1534G=
ENST00000299427.10:c.514G=	ENSP00000299427.6:p.Gly172=
ENST00000428886.6:n.683G=
ENST00000436873.6:c.450+211G=	ENSP00000398136.2:n.450+211G=
ENST00000524788.1:n.214G=
ENST00000528571.5:c.*254G=	ENSP00000434647.1:n.*254G=
ENST00000528807.1:n.64G=
ENST00000533371.5:c.-216G=	ENSP00000437066.1:n.-216G=
ENST00000534644.5:n.499G=
ENST00000611494.4:c.514G=	ENSP00000484546.1:p.Gly172=
NM_000391.3:c.514G=	NP_000382.3:p.Gly172=
NM_000391.4:c.514G= MANE Select	NP_000382.3:p.Gly172=