Canonical Allele Identifier: CA379472932

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6636710C>A (hg19) ; chr11:g.6615479C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615479C>A , CM000673.2:g.6615479C>A	GRCh38
NC_000011.9:g.6636710C>A , CM000673.1:g.6636710C>A	GRCh37
NC_000011.8:g.6593286C>A	NCBI36
NG_008653.1:g.8983G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1115G>T	ENSP00000507321.1:p.Gly372Val
ENST00000299427.12:c.1229G>T MANE Select	ENSP00000299427.6:p.Gly410Val
ENST00000436873.7:c.466G>T
ENST00000524924.2:n.349G>T
ENST00000533371.6:c.500G>T	ENSP00000437066.1:p.Gly167Val
ENST00000642892.1:c.500G>T	ENSP00000494165.1:p.Gly167Val
ENST00000643342.1:c.302G>T
ENST00000643439.1:c.*969G>T	ENSP00000495849.1:n.*969G>T
ENST00000643479.1:n.1415G>T
ENST00000643516.1:c.738G>T
ENST00000644218.1:c.1040G>T	ENSP00000493574.1:p.Gly347Val
ENST00000644683.1:c.*682G>T	ENSP00000494085.1:n.*682G>T
ENST00000644810.1:c.950G>T	ENSP00000495895.1:p.Gly317Val
ENST00000644831.1:n.1405G>T
ENST00000644933.1:c.*95G>T	ENSP00000496133.1:n.*95G>T
ENST00000645285.1:c.*95G>T	ENSP00000495058.1:n.*95G>T
ENST00000645331.1:n.2434G>T
ENST00000645620.1:c.500G>T	ENSP00000493657.1:p.Gly167Val
ENST00000646691.1:n.1004G>T
ENST00000646777.1:n.1562G>T
ENST00000647016.1:n.1709G>T
ENST00000647152.1:c.500G>T	ENSP00000495893.1:p.Gly167Val
ENST00000647209.1:c.*1098G>T	ENSP00000495558.1:n.*1098G>T
ENST00000647346.1:n.2249G>T
ENST00000299427.10:c.1229G>T	ENSP00000299427.6:p.Gly410Val
ENST00000524924.1:n.184G>T
ENST00000532191.1:n.282G>T
ENST00000533371.5:c.500G>T	ENSP00000437066.1:p.Gly167Val
ENST00000611494.4:c.1229G>T	ENSP00000484546.1:p.Gly410Val
NM_000391.3:c.1229G>T	NP_000382.3:p.Gly410Val
NM_000391.4:c.1229G>T MANE Select	NP_000382.3:p.Gly410Val