Canonical Allele Identifier: CA1950232693

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6614623C= , CM000673.2:g.6614623C=	GRCh38
NC_000011.9:g.6635854C= , CM000673.1:g.6635854C=	GRCh37
NC_000011.8:g.6592430C=	NCBI36
NG_008653.1:g.9839G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1501G=	ENSP00000507321.1:p.Gly501=
ENST00000299427.12:c.1615G= MANE Select	ENSP00000299427.6:p.Gly539=
ENST00000524611.2:n.654G=
ENST00000524924.2:n.735G=
ENST00000533371.6:c.886G=	ENSP00000437066.1:p.Gly296=
ENST00000642892.1:c.886G=	ENSP00000494165.1:p.Gly296=
ENST00000643342.1:c.688G=
ENST00000643439.1:c.*1355G=	ENSP00000495849.1:n.*1355G=
ENST00000643479.1:n.1801G=
ENST00000643516.1:c.1124G=
ENST00000644218.1:c.1426G=	ENSP00000493574.1:p.Gly476=
ENST00000644683.1:c.*1068G=	ENSP00000494085.1:n.*1068G=
ENST00000644810.1:c.1336G=	ENSP00000495895.1:p.Gly446=
ENST00000644831.1:n.1791G=
ENST00000644933.1:c.*481G=	ENSP00000496133.1:n.*481G=
ENST00000645285.1:c.*481G=	ENSP00000495058.1:n.*481G=
ENST00000645331.1:n.2820G=
ENST00000645620.1:c.886G=	ENSP00000493657.1:p.Gly296=
ENST00000646691.1:n.1502G=
ENST00000646777.1:n.1948G=
ENST00000647016.1:n.2095G=
ENST00000647152.1:c.886G=	ENSP00000495893.1:p.Gly296=
ENST00000647209.1:c.*1484G=	ENSP00000495558.1:n.*1484G=
ENST00000647346.1:n.2635G=
ENST00000299427.10:c.1615G=	ENSP00000299427.6:p.Gly539=
ENST00000533371.5:c.886G=	ENSP00000437066.1:p.Gly296=
ENST00000611494.4:c.1615G=	ENSP00000484546.1:p.Gly539=
NM_000391.3:c.1615G=	NP_000382.3:p.Gly539=
NM_000391.4:c.1615G= MANE Select	NP_000382.3:p.Gly539=