Canonical Allele Identifier: CA5858944

Gene: TPP1

Linked Data

• ClinVar Variation Id: 859613
• ClinVar RCV Id: RCV002265936 ; RCV002497463
• dbSNP Id: rs764256845
• ExAC: 11:6638559 G / A
• gnomAD v2: 11-6638559-G-A
• gnomAD v4: 11-6617328-G-A
• MyVariant Identifiers: chr11:g.6638559G>A (hg19) ; chr11:g.6617328G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617328G>A , CM000673.2:g.6617328G>A	GRCh38
NC_000011.9:g.6638559G>A , CM000673.1:g.6638559G>A	GRCh37
NC_000011.8:g.6595135G>A	NCBI36
NG_008653.1:g.7134C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.367C>T	ENSP00000507321.1:p.Gln123Ter
ENST00000299427.12:c.481C>T MANE Select	ENSP00000299427.6:p.Gln161Ter
ENST00000428886.7:n.569C>T
ENST00000436873.7:c.285C>T
ENST00000524788.2:n.1493C>T
ENST00000524903.2:n.1609C>T
ENST00000528571.6:c.*221C>T	ENSP00000434647.1:n.*221C>T
ENST00000528807.2:n.137C>T
ENST00000530040.2:n.479+31C>T
ENST00000533371.6:c.-249C>T	ENSP00000437066.1:n.-249C>T
ENST00000534644.6:n.456+26C>T
ENST00000642892.1:c.-222+26C>T	ENSP00000494165.1:n.-222+26C>T
ENST00000643439.1:c.*221C>T	ENSP00000495849.1:n.*221C>T
ENST00000643479.1:n.510C>T
ENST00000643516.1:c.368C>T
ENST00000644151.1:n.1773C>T
ENST00000644218.1:c.481C>T	ENSP00000493574.1:p.Gln161Ter
ENST00000644683.1:c.450+31C>T	ENSP00000494085.1:n.450+31C>T
ENST00000644810.1:c.230-175C>T	ENSP00000495895.1:n.230-175C>T
ENST00000644831.1:n.510C>T
ENST00000644933.1:c.-249C>T	ENSP00000496133.1:n.-249C>T
ENST00000645020.1:n.1509C>T
ENST00000645285.1:c.-249C>T	ENSP00000495058.1:n.-249C>T
ENST00000645331.1:n.700C>T
ENST00000645620.1:c.-222+31C>T	ENSP00000493657.1:n.-222+31C>T
ENST00000646777.1:n.510C>T
ENST00000647016.1:n.814C>T
ENST00000647152.1:c.-249C>T	ENSP00000495893.1:n.-249C>T
ENST00000647209.1:c.*350C>T	ENSP00000495558.1:n.*350C>T
ENST00000647346.1:n.1501C>T
ENST00000299427.10:c.481C>T	ENSP00000299427.6:p.Gln161Ter
ENST00000428886.6:n.503C>T
ENST00000436873.6:c.450+31C>T	ENSP00000398136.2:n.450+31C>T
ENST00000524788.1:n.34C>T
ENST00000528571.5:c.*221C>T	ENSP00000434647.1:n.*221C>T
ENST00000533371.5:c.-249C>T	ENSP00000437066.1:n.-249C>T
ENST00000534644.5:n.466C>T
ENST00000611494.4:c.481C>T	ENSP00000484546.1:p.Gln161Ter
NM_000391.3:c.481C>T	NP_000382.3:p.Gln161Ter
NM_000391.4:c.481C>T MANE Select	NP_000382.3:p.Gln161Ter