Canonical Allele Identifier: CA379475311

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638211C>G (hg19) ; chr11:g.6616980C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616980C>G , CM000673.2:g.6616980C>G	GRCh38
NC_000011.9:g.6638211C>G , CM000673.1:g.6638211C>G	GRCh37
NC_000011.8:g.6594787C>G	NCBI36
NG_008653.1:g.7482G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.568G>C	ENSP00000507321.1:p.Ala190Pro
ENST00000299427.12:c.682G>C MANE Select	ENSP00000299427.6:p.Ala228Pro
ENST00000436873.7:c.312+321G>C
ENST00000524788.2:n.1841G>C
ENST00000524903.2:n.1957G>C
ENST00000528807.2:n.338G>C
ENST00000530040.2:n.479+379G>C
ENST00000533371.6:c.-48G>C	ENSP00000437066.1:n.-48G>C
ENST00000534644.6:n.630G>C
ENST00000642892.1:c.-48G>C	ENSP00000494165.1:n.-48G>C
ENST00000643439.1:c.*422G>C	ENSP00000495849.1:n.*422G>C
ENST00000643479.1:n.711G>C
ENST00000643516.1:c.395+321G>C
ENST00000644151.1:n.2121G>C
ENST00000644218.1:c.682G>C	ENSP00000493574.1:p.Ala228Pro
ENST00000644683.1:c.*135G>C	ENSP00000494085.1:n.*135G>C
ENST00000644810.1:c.403G>C	ENSP00000495895.1:p.Ala135Pro
ENST00000644831.1:n.858G>C
ENST00000644933.1:c.-48G>C	ENSP00000496133.1:n.-48G>C
ENST00000645020.1:n.1857G>C
ENST00000645285.1:c.-48G>C	ENSP00000495058.1:n.-48G>C
ENST00000645331.1:n.1048G>C
ENST00000645620.1:c.-48G>C	ENSP00000493657.1:n.-48G>C
ENST00000646777.1:n.858G>C
ENST00000647016.1:n.1162G>C
ENST00000647152.1:c.-48G>C	ENSP00000495893.1:n.-48G>C
ENST00000647209.1:c.*551G>C	ENSP00000495558.1:n.*551G>C
ENST00000647346.1:n.1702G>C
ENST00000299427.10:c.682G>C	ENSP00000299427.6:p.Ala228Pro
ENST00000436873.6:c.450+379G>C	ENSP00000398136.2:n.450+379G>C
ENST00000524788.1:n.382G>C
ENST00000528807.1:n.232G>C
ENST00000533371.5:c.-48G>C	ENSP00000437066.1:n.-48G>C
ENST00000611494.4:c.682G>C	ENSP00000484546.1:p.Ala228Pro
NM_000391.3:c.682G>C	NP_000382.3:p.Ala228Pro
NM_000391.4:c.682G>C MANE Select	NP_000382.3:p.Ala228Pro