Canonical Allele Identifier: CA472922995

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638919G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617688G>T , CM000673.2:g.6617688G>T	GRCh38
NC_000011.9:g.6638919G>T , CM000673.1:g.6638919G>T	GRCh37
NC_000011.8:g.6595495G>T	NCBI36
NG_008653.1:g.6774C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.204C>A	ENSP00000507321.1:p.Ala68=
ENST00000299427.12:c.318C>A MANE Select	ENSP00000299427.6:p.Ala106=
ENST00000428886.7:n.406C>A
ENST00000436873.7:c.122C>A
ENST00000524788.2:n.1330C>A
ENST00000524903.2:n.1446C>A
ENST00000528571.6:c.*58C>A	ENSP00000434647.1:n.*58C>A
ENST00000530040.2:n.347C>A
ENST00000533371.6:c.-412C>A	ENSP00000437066.1:n.-412C>A
ENST00000534644.6:n.319C>A
ENST00000642892.1:c.-359C>A	ENSP00000494165.1:n.-359C>A
ENST00000643439.1:c.*58C>A	ENSP00000495849.1:n.*58C>A
ENST00000643479.1:n.347C>A
ENST00000643516.1:c.205C>A
ENST00000644151.1:n.1610C>A
ENST00000644218.1:c.318C>A	ENSP00000493574.1:p.Ala106=
ENST00000644683.1:c.318C>A	ENSP00000494085.1:p.Ala106=
ENST00000644810.1:c.230-535C>A	ENSP00000495895.1:n.230-535C>A
ENST00000644831.1:n.347C>A
ENST00000644933.1:c.-412C>A	ENSP00000496133.1:n.-412C>A
ENST00000645020.1:n.1346C>A
ENST00000645285.1:c.-412C>A	ENSP00000495058.1:n.-412C>A
ENST00000645331.1:n.340C>A
ENST00000645620.1:c.-354C>A	ENSP00000493657.1:n.-354C>A
ENST00000646777.1:n.347C>A
ENST00000647016.1:n.651C>A
ENST00000647152.1:c.-412C>A	ENSP00000495893.1:n.-412C>A
ENST00000647209.1:c.*187C>A	ENSP00000495558.1:n.*187C>A
ENST00000647346.1:n.1338C>A
ENST00000299427.10:c.318C>A	ENSP00000299427.6:p.Ala106=
ENST00000428886.6:n.340C>A
ENST00000436873.6:c.318C>A	ENSP00000398136.2:p.Ala106=
ENST00000528571.5:c.*58C>A	ENSP00000434647.1:n.*58C>A
ENST00000530040.1:n.430C>A
ENST00000533371.5:c.-412C>A	ENSP00000437066.1:n.-412C>A
ENST00000534644.5:n.303C>A
ENST00000611494.4:c.318C>A	ENSP00000484546.1:p.Ala106=
NM_000391.3:c.318C>A	NP_000382.3:p.Ala106=
NM_000391.4:c.318C>A MANE Select	NP_000382.3:p.Ala106=