Canonical Allele Identifier: CA2612258116

Gene: TPP1

Linked Data

• gnomAD v4: 11-6616641-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616641T>G , CM000673.2:g.6616641T>G	GRCh38
NC_000011.9:g.6637872T>G , CM000673.1:g.6637872T>G	GRCh37
NC_000011.8:g.6594448T>G	NCBI36
NG_008653.1:g.7821A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.772+20A>C	ENSP00000507321.1:n.772+20A>C
ENST00000299427.12:c.886+20A>C MANE Select	ENSP00000299427.6:n.886+20A>C
ENST00000436873.7:c.313-567A>C
ENST00000524788.2:n.2065A>C
ENST00000524903.2:n.2181A>C
ENST00000528807.2:n.562A>C
ENST00000530040.2:n.480-138A>C
ENST00000533371.6:c.157+20A>C	ENSP00000437066.1:n.157+20A>C
ENST00000642892.1:c.157+20A>C	ENSP00000494165.1:n.157+20A>C
ENST00000643439.1:c.*626+20A>C	ENSP00000495849.1:n.*626+20A>C
ENST00000643479.1:n.935A>C
ENST00000643516.1:c.396-138A>C
ENST00000644218.1:c.886+20A>C	ENSP00000493574.1:n.886+20A>C
ENST00000644683.1:c.*339+20A>C	ENSP00000494085.1:n.*339+20A>C
ENST00000644810.1:c.607+20A>C	ENSP00000495895.1:n.607+20A>C
ENST00000644831.1:n.1062+20A>C
ENST00000644933.1:c.157+20A>C	ENSP00000496133.1:n.157+20A>C
ENST00000645020.1:n.2196A>C
ENST00000645285.1:c.157+20A>C	ENSP00000495058.1:n.157+20A>C
ENST00000645331.1:n.1272A>C
ENST00000645620.1:c.157+20A>C	ENSP00000493657.1:n.157+20A>C
ENST00000646777.1:n.1082A>C
ENST00000647016.1:n.1366+20A>C
ENST00000647152.1:c.157+20A>C	ENSP00000495893.1:n.157+20A>C
ENST00000647209.1:c.*755+20A>C	ENSP00000495558.1:n.*755+20A>C
ENST00000647346.1:n.1906+20A>C
ENST00000299427.10:c.886+20A>C	ENSP00000299427.6:n.886+20A>C
ENST00000436873.6:c.451-138A>C	ENSP00000398136.2:n.451-138A>C
ENST00000528807.1:n.456A>C
ENST00000533371.5:c.157+20A>C	ENSP00000437066.1:n.157+20A>C
ENST00000611494.4:c.886+20A>C	ENSP00000484546.1:n.886+20A>C
NM_000391.3:c.886+20A>C	NP_000382.3:n.886+20A>C
NM_000391.4:c.886+20A>C MANE Select	NP_000382.3:n.886+20A>C