Canonical Allele Identifier: CA379475930

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638613C>A (hg19) ; chr11:g.6617382C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617382C>A , CM000673.2:g.6617382C>A	GRCh38
NC_000011.9:g.6638613C>A , CM000673.1:g.6638613C>A	GRCh37
NC_000011.8:g.6595189C>A	NCBI36
NG_008653.1:g.7080G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.313G>T	ENSP00000507321.1:p.Gly105Ter
ENST00000299427.12:c.427G>T MANE Select	ENSP00000299427.6:p.Gly143Ter
ENST00000428886.7:n.515G>T
ENST00000436873.7:c.231G>T
ENST00000524788.2:n.1439G>T
ENST00000524903.2:n.1555G>T
ENST00000528571.6:c.*167G>T	ENSP00000434647.1:n.*167G>T
ENST00000528807.2:n.83G>T
ENST00000530040.2:n.456G>T
ENST00000533371.6:c.-303G>T	ENSP00000437066.1:n.-303G>T
ENST00000534644.6:n.428G>T
ENST00000642892.1:c.-250G>T	ENSP00000494165.1:n.-250G>T
ENST00000643439.1:c.*167G>T	ENSP00000495849.1:n.*167G>T
ENST00000643479.1:n.456G>T
ENST00000643516.1:c.314G>T
ENST00000644151.1:n.1719G>T
ENST00000644218.1:c.427G>T	ENSP00000493574.1:p.Gly143Ter
ENST00000644683.1:c.427G>T	ENSP00000494085.1:p.Gly143Ter
ENST00000644810.1:c.230-229G>T	ENSP00000495895.1:n.230-229G>T
ENST00000644831.1:n.456G>T
ENST00000644933.1:c.-303G>T	ENSP00000496133.1:n.-303G>T
ENST00000645020.1:n.1455G>T
ENST00000645285.1:c.-303G>T	ENSP00000495058.1:n.-303G>T
ENST00000645331.1:n.646G>T
ENST00000645620.1:c.-245G>T	ENSP00000493657.1:n.-245G>T
ENST00000646777.1:n.456G>T
ENST00000647016.1:n.760G>T
ENST00000647152.1:c.-303G>T	ENSP00000495893.1:n.-303G>T
ENST00000647209.1:c.*296G>T	ENSP00000495558.1:n.*296G>T
ENST00000647346.1:n.1447G>T
ENST00000299427.10:c.427G>T	ENSP00000299427.6:p.Gly143Ter
ENST00000428886.6:n.449G>T
ENST00000436873.6:c.427G>T	ENSP00000398136.2:p.Gly143Ter
ENST00000528571.5:c.*167G>T	ENSP00000434647.1:n.*167G>T
ENST00000530040.1:n.539G>T
ENST00000533371.5:c.-303G>T	ENSP00000437066.1:n.-303G>T
ENST00000534644.5:n.412G>T
ENST00000611494.4:c.427G>T	ENSP00000484546.1:p.Gly143Ter
NM_000391.3:c.427G>T	NP_000382.3:p.Gly143Ter
NM_000391.4:c.427G>T MANE Select	NP_000382.3:p.Gly143Ter