Canonical Allele Identifier: CA379475362

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638232T>G (hg19) ; chr11:g.6617001T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617001T>G , CM000673.2:g.6617001T>G	GRCh38
NC_000011.9:g.6638232T>G , CM000673.1:g.6638232T>G	GRCh37
NC_000011.8:g.6594808T>G	NCBI36
NG_008653.1:g.7461A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.547A>C	ENSP00000507321.1:p.Ser183Arg
ENST00000299427.12:c.661A>C MANE Select	ENSP00000299427.6:p.Ser221Arg
ENST00000436873.7:c.312+300A>C
ENST00000524788.2:n.1820A>C
ENST00000524903.2:n.1936A>C
ENST00000528807.2:n.317A>C
ENST00000530040.2:n.479+358A>C
ENST00000533371.6:c.-69A>C	ENSP00000437066.1:n.-69A>C
ENST00000534644.6:n.609A>C
ENST00000642892.1:c.-69A>C	ENSP00000494165.1:n.-69A>C
ENST00000643439.1:c.*401A>C	ENSP00000495849.1:n.*401A>C
ENST00000643479.1:n.690A>C
ENST00000643516.1:c.395+300A>C
ENST00000644151.1:n.2100A>C
ENST00000644218.1:c.661A>C	ENSP00000493574.1:p.Ser221Arg
ENST00000644683.1:c.*114A>C	ENSP00000494085.1:n.*114A>C
ENST00000644810.1:c.382A>C	ENSP00000495895.1:p.Ser128Arg
ENST00000644831.1:n.837A>C
ENST00000644933.1:c.-69A>C	ENSP00000496133.1:n.-69A>C
ENST00000645020.1:n.1836A>C
ENST00000645285.1:c.-69A>C	ENSP00000495058.1:n.-69A>C
ENST00000645331.1:n.1027A>C
ENST00000645620.1:c.-69A>C	ENSP00000493657.1:n.-69A>C
ENST00000646777.1:n.837A>C
ENST00000647016.1:n.1141A>C
ENST00000647152.1:c.-69A>C	ENSP00000495893.1:n.-69A>C
ENST00000647209.1:c.*530A>C	ENSP00000495558.1:n.*530A>C
ENST00000647346.1:n.1681A>C
ENST00000299427.10:c.661A>C	ENSP00000299427.6:p.Ser221Arg
ENST00000428886.6:n.830A>C
ENST00000436873.6:c.450+358A>C	ENSP00000398136.2:n.450+358A>C
ENST00000524788.1:n.361A>C
ENST00000528571.5:c.*401A>C	ENSP00000434647.1:n.*401A>C
ENST00000528807.1:n.211A>C
ENST00000533371.5:c.-69A>C	ENSP00000437066.1:n.-69A>C
ENST00000611494.4:c.661A>C	ENSP00000484546.1:p.Ser221Arg
NM_000391.3:c.661A>C	NP_000382.3:p.Ser221Arg
NM_000391.4:c.661A>C MANE Select	NP_000382.3:p.Ser221Arg