Canonical Allele Identifier: CA1950234541

Gene: TPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615442C= , CM000673.2:g.6615442C=	GRCh38
NC_000011.9:g.6636673C= , CM000673.1:g.6636673C=	GRCh37
NC_000011.8:g.6593249C=	NCBI36
NG_008653.1:g.9020G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1152G=	ENSP00000507321.1:p.Gln384=
ENST00000299427.12:c.1266G= MANE Select	ENSP00000299427.6:p.Gln422=
ENST00000436873.7:c.503G=
ENST00000524611.2:n.14G=
ENST00000524924.2:n.386G=
ENST00000533371.6:c.537G=	ENSP00000437066.1:p.Gln179=
ENST00000642892.1:c.537G=	ENSP00000494165.1:p.Gln179=
ENST00000643342.1:c.339G=
ENST00000643439.1:c.*1006G=	ENSP00000495849.1:n.*1006G=
ENST00000643479.1:n.1452G=
ENST00000643516.1:c.775G=
ENST00000644218.1:c.1077G=	ENSP00000493574.1:p.Gln359=
ENST00000644683.1:c.*719G=	ENSP00000494085.1:n.*719G=
ENST00000644810.1:c.987G=	ENSP00000495895.1:p.Gln329=
ENST00000644831.1:n.1442G=
ENST00000644933.1:c.*132G=	ENSP00000496133.1:n.*132G=
ENST00000645285.1:c.*132G=	ENSP00000495058.1:n.*132G=
ENST00000645331.1:n.2471G=
ENST00000645620.1:c.537G=	ENSP00000493657.1:p.Gln179=
ENST00000646691.1:n.1041G=
ENST00000646777.1:n.1599G=
ENST00000647016.1:n.1746G=
ENST00000647152.1:c.537G=	ENSP00000495893.1:p.Gln179=
ENST00000647209.1:c.*1135G=	ENSP00000495558.1:n.*1135G=
ENST00000647346.1:n.2286G=
ENST00000299427.10:c.1266G=	ENSP00000299427.6:p.Gln422=
ENST00000524611.1:n.32G=
ENST00000524924.1:n.221G=
ENST00000532191.1:n.319G=
ENST00000533371.5:c.537G=	ENSP00000437066.1:p.Gln179=
ENST00000611494.4:c.1266G=	ENSP00000484546.1:p.Gln422=
NM_000391.3:c.1266G=	NP_000382.3:p.Gln422=
NM_000391.4:c.1266G= MANE Select	NP_000382.3:p.Gln422=