Canonical Allele Identifier: CA1950234654

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615491T= , CM000673.2:g.6615491T=	GRCh38
NC_000011.9:g.6636722T= , CM000673.1:g.6636722T=	GRCh37
NC_000011.8:g.6593298T=	NCBI36
NG_008653.1:g.8971A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1103A=	ENSP00000507321.1:p.Tyr368=
ENST00000299427.12:c.1217A= MANE Select	ENSP00000299427.6:p.Tyr406=
ENST00000436873.7:c.454A=
ENST00000524924.2:n.337A=
ENST00000533371.6:c.488A=	ENSP00000437066.1:p.Tyr163=
ENST00000642892.1:c.488A=	ENSP00000494165.1:p.Tyr163=
ENST00000643342.1:c.290A=
ENST00000643439.1:c.*957A=	ENSP00000495849.1:n.*957A=
ENST00000643479.1:n.1403A=
ENST00000643516.1:c.726A=
ENST00000644218.1:c.1028A=	ENSP00000493574.1:p.Tyr343=
ENST00000644683.1:c.*670A=	ENSP00000494085.1:n.*670A=
ENST00000644810.1:c.938A=	ENSP00000495895.1:p.Tyr313=
ENST00000644831.1:n.1393A=
ENST00000644933.1:c.*83A=	ENSP00000496133.1:n.*83A=
ENST00000645285.1:c.*83A=	ENSP00000495058.1:n.*83A=
ENST00000645331.1:n.2422A=
ENST00000645620.1:c.488A=	ENSP00000493657.1:p.Tyr163=
ENST00000646691.1:n.992A=
ENST00000646777.1:n.1550A=
ENST00000647016.1:n.1697A=
ENST00000647152.1:c.488A=	ENSP00000495893.1:p.Tyr163=
ENST00000647209.1:c.*1086A=	ENSP00000495558.1:n.*1086A=
ENST00000647346.1:n.2237A=
ENST00000299427.10:c.1217A=	ENSP00000299427.6:p.Tyr406=
ENST00000524924.1:n.172A=
ENST00000532191.1:n.270A=
ENST00000533371.5:c.488A=	ENSP00000437066.1:p.Tyr163=
ENST00000611494.4:c.1217A=	ENSP00000484546.1:p.Tyr406=
NM_000391.3:c.1217A=	NP_000382.3:p.Tyr406=
NM_000391.4:c.1217A= MANE Select	NP_000382.3:p.Tyr406=