Canonical Allele Identifier: CA1950234553

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615447A= , CM000673.2:g.6615447A=	GRCh38
NC_000011.9:g.6636678A= , CM000673.1:g.6636678A=	GRCh37
NC_000011.8:g.6593254A=	NCBI36
NG_008653.1:g.9015T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1147T=	ENSP00000507321.1:p.Tyr383=
ENST00000299427.12:c.1261T= MANE Select	ENSP00000299427.6:p.Tyr421=
ENST00000436873.7:c.498T=
ENST00000524611.2:n.9T=
ENST00000524924.2:n.381T=
ENST00000533371.6:c.532T=	ENSP00000437066.1:p.Tyr178=
ENST00000642892.1:c.532T=	ENSP00000494165.1:p.Tyr178=
ENST00000643342.1:c.334T=
ENST00000643439.1:c.*1001T=	ENSP00000495849.1:n.*1001T=
ENST00000643479.1:n.1447T=
ENST00000643516.1:c.770T=
ENST00000644218.1:c.1072T=	ENSP00000493574.1:p.Tyr358=
ENST00000644683.1:c.*714T=	ENSP00000494085.1:n.*714T=
ENST00000644810.1:c.982T=	ENSP00000495895.1:p.Tyr328=
ENST00000644831.1:n.1437T=
ENST00000644933.1:c.*127T=	ENSP00000496133.1:n.*127T=
ENST00000645285.1:c.*127T=	ENSP00000495058.1:n.*127T=
ENST00000645331.1:n.2466T=
ENST00000645620.1:c.532T=	ENSP00000493657.1:p.Tyr178=
ENST00000646691.1:n.1036T=
ENST00000646777.1:n.1594T=
ENST00000647016.1:n.1741T=
ENST00000647152.1:c.532T=	ENSP00000495893.1:p.Tyr178=
ENST00000647209.1:c.*1130T=	ENSP00000495558.1:n.*1130T=
ENST00000647346.1:n.2281T=
ENST00000299427.10:c.1261T=	ENSP00000299427.6:p.Tyr421=
ENST00000524611.1:n.27T=
ENST00000524924.1:n.216T=
ENST00000532191.1:n.314T=
ENST00000533371.5:c.532T=	ENSP00000437066.1:p.Tyr178=
ENST00000611494.4:c.1261T=	ENSP00000484546.1:p.Tyr421=
NM_000391.3:c.1261T=	NP_000382.3:p.Tyr421=
NM_000391.4:c.1261T= MANE Select	NP_000382.3:p.Tyr421=