Canonical Allele Identifier: CA379476043

Gene: TPP1

Linked Data

• dbSNP Id: rs1855604108
• MyVariant Identifiers: chr11:g.6638645A>G (hg19) ; chr11:g.6617414A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617414A>G , CM000673.2:g.6617414A>G	GRCh38
NC_000011.9:g.6638645A>G , CM000673.1:g.6638645A>G	GRCh37
NC_000011.8:g.6595221A>G	NCBI36
NG_008653.1:g.7048T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.281T>C	ENSP00000507321.1:p.Leu94Pro
ENST00000299427.12:c.395T>C MANE Select	ENSP00000299427.6:p.Leu132Pro
ENST00000428886.7:n.483T>C
ENST00000436873.7:c.199T>C
ENST00000524788.2:n.1407T>C
ENST00000524903.2:n.1523T>C
ENST00000528571.6:c.*135T>C	ENSP00000434647.1:n.*135T>C
ENST00000528807.2:n.51T>C
ENST00000530040.2:n.424T>C
ENST00000533371.6:c.-335T>C	ENSP00000437066.1:n.-335T>C
ENST00000534644.6:n.396T>C
ENST00000642892.1:c.-282T>C	ENSP00000494165.1:n.-282T>C
ENST00000643439.1:c.*135T>C	ENSP00000495849.1:n.*135T>C
ENST00000643479.1:n.424T>C
ENST00000643516.1:c.282T>C
ENST00000644151.1:n.1687T>C
ENST00000644218.1:c.395T>C	ENSP00000493574.1:p.Leu132Pro
ENST00000644683.1:c.395T>C	ENSP00000494085.1:p.Leu132Pro
ENST00000644810.1:c.230-261T>C	ENSP00000495895.1:n.230-261T>C
ENST00000644831.1:n.424T>C
ENST00000644933.1:c.-335T>C	ENSP00000496133.1:n.-335T>C
ENST00000645020.1:n.1423T>C
ENST00000645285.1:c.-335T>C	ENSP00000495058.1:n.-335T>C
ENST00000645331.1:n.614T>C
ENST00000645620.1:c.-277T>C	ENSP00000493657.1:n.-277T>C
ENST00000646777.1:n.424T>C
ENST00000647016.1:n.728T>C
ENST00000647152.1:c.-335T>C	ENSP00000495893.1:n.-335T>C
ENST00000647209.1:c.*264T>C	ENSP00000495558.1:n.*264T>C
ENST00000647346.1:n.1415T>C
ENST00000299427.10:c.395T>C	ENSP00000299427.6:p.Leu132Pro
ENST00000428886.6:n.417T>C
ENST00000436873.6:c.395T>C	ENSP00000398136.2:p.Leu132Pro
ENST00000528571.5:c.*135T>C	ENSP00000434647.1:n.*135T>C
ENST00000530040.1:n.507T>C
ENST00000533371.5:c.-335T>C	ENSP00000437066.1:n.-335T>C
ENST00000534644.5:n.380T>C
ENST00000611494.4:c.395T>C	ENSP00000484546.1:p.Leu132Pro
NM_000391.3:c.395T>C	NP_000382.3:p.Leu132Pro
NM_000391.4:c.395T>C MANE Select	NP_000382.3:p.Leu132Pro