Canonical Allele Identifier: CA472922942

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638287G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617056G>T , CM000673.2:g.6617056G>T	GRCh38
NC_000011.9:g.6638287G>T , CM000673.1:g.6638287G>T	GRCh37
NC_000011.8:g.6594863G>T	NCBI36
NG_008653.1:g.7406C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.492C>A	ENSP00000507321.1:p.Pro164=
ENST00000299427.12:c.606C>A MANE Select	ENSP00000299427.6:p.Pro202=
ENST00000436873.7:c.312+245C>A
ENST00000524788.2:n.1765C>A
ENST00000524903.2:n.1881C>A
ENST00000528807.2:n.262C>A
ENST00000530040.2:n.479+303C>A
ENST00000533371.6:c.-124C>A	ENSP00000437066.1:n.-124C>A
ENST00000534644.6:n.554C>A
ENST00000642892.1:c.-124C>A	ENSP00000494165.1:n.-124C>A
ENST00000643439.1:c.*346C>A	ENSP00000495849.1:n.*346C>A
ENST00000643479.1:n.635C>A
ENST00000643516.1:c.395+245C>A
ENST00000644151.1:n.2045C>A
ENST00000644218.1:c.606C>A	ENSP00000493574.1:p.Pro202=
ENST00000644683.1:c.*59C>A	ENSP00000494085.1:n.*59C>A
ENST00000644810.1:c.327C>A	ENSP00000495895.1:p.Pro109=
ENST00000644831.1:n.782C>A
ENST00000644933.1:c.-124C>A	ENSP00000496133.1:n.-124C>A
ENST00000645020.1:n.1781C>A
ENST00000645285.1:c.-124C>A	ENSP00000495058.1:n.-124C>A
ENST00000645331.1:n.972C>A
ENST00000645620.1:c.-124C>A	ENSP00000493657.1:n.-124C>A
ENST00000646777.1:n.782C>A
ENST00000647016.1:n.1086C>A
ENST00000647152.1:c.-124C>A	ENSP00000495893.1:n.-124C>A
ENST00000647209.1:c.*475C>A	ENSP00000495558.1:n.*475C>A
ENST00000647346.1:n.1626C>A
ENST00000299427.10:c.606C>A	ENSP00000299427.6:p.Pro202=
ENST00000428886.6:n.775C>A
ENST00000436873.6:c.450+303C>A	ENSP00000398136.2:n.450+303C>A
ENST00000524788.1:n.306C>A
ENST00000528571.5:c.*346C>A	ENSP00000434647.1:n.*346C>A
ENST00000528807.1:n.156C>A
ENST00000533371.5:c.-124C>A	ENSP00000437066.1:n.-124C>A
ENST00000534644.5:n.591C>A
ENST00000611494.4:c.606C>A	ENSP00000484546.1:p.Pro202=
NM_000391.3:c.606C>A	NP_000382.3:p.Pro202=
NM_000391.4:c.606C>A MANE Select	NP_000382.3:p.Pro202=