Canonical Allele Identifier: CA1950233882

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615189T= , CM000673.2:g.6615189T=	GRCh38
NC_000011.9:g.6636420T= , CM000673.1:g.6636420T=	GRCh37
NC_000011.8:g.6592996T=	NCBI36
NG_008653.1:g.9273A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1293A=	ENSP00000507321.1:p.Pro431=
ENST00000299427.12:c.1407A= MANE Select	ENSP00000299427.6:p.Pro469=
ENST00000524611.2:n.267A=
ENST00000524924.2:n.527A=
ENST00000533371.6:c.678A=	ENSP00000437066.1:p.Pro226=
ENST00000642892.1:c.678A=	ENSP00000494165.1:p.Pro226=
ENST00000643342.1:c.480A=
ENST00000643439.1:c.*1147A=	ENSP00000495849.1:n.*1147A=
ENST00000643479.1:n.1593A=
ENST00000643516.1:c.916A=
ENST00000644218.1:c.1218A=	ENSP00000493574.1:p.Pro406=
ENST00000644683.1:c.*860A=	ENSP00000494085.1:n.*860A=
ENST00000644810.1:c.1128A=	ENSP00000495895.1:p.Pro376=
ENST00000644831.1:n.1583A=
ENST00000644933.1:c.*273A=	ENSP00000496133.1:n.*273A=
ENST00000645285.1:c.*273A=	ENSP00000495058.1:n.*273A=
ENST00000645331.1:n.2612A=
ENST00000645620.1:c.678A=	ENSP00000493657.1:p.Pro226=
ENST00000646691.1:n.1294A=
ENST00000646777.1:n.1740A=
ENST00000647016.1:n.1887A=
ENST00000647152.1:c.678A=	ENSP00000495893.1:p.Pro226=
ENST00000647209.1:c.*1276A=	ENSP00000495558.1:n.*1276A=
ENST00000647346.1:n.2427A=
ENST00000299427.10:c.1407A=	ENSP00000299427.6:p.Pro469=
ENST00000524611.1:n.285A=
ENST00000533371.5:c.678A=	ENSP00000437066.1:p.Pro226=
ENST00000611494.4:c.1407A=	ENSP00000484546.1:p.Pro469=
NM_000391.3:c.1407A=	NP_000382.3:p.Pro469=
NM_000391.4:c.1407A= MANE Select	NP_000382.3:p.Pro469=