Canonical Allele Identifier: CA679351906

Gene: TPP1

Linked Data

• dbSNP Id: rs1390577489
• gnomAD v3: 11-6617992-C-A
• gnomAD v4: 11-6617992-C-A
• MyVariant Identifiers: chr11:g.6639223C>A (hg19) ; chr11:g.6617992C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617992C>A , CM000673.2:g.6617992C>A	GRCh38
NC_000011.9:g.6639223C>A , CM000673.1:g.6639223C>A	GRCh37
NC_000011.8:g.6595799C>A	NCBI36
NG_008653.1:g.6470G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.116-216G>T	ENSP00000507321.1:n.116-216G>T
ENST00000299427.12:c.230-216G>T MANE Select	ENSP00000299427.6:n.230-216G>T
ENST00000428886.7:n.318-216G>T
ENST00000436873.7:c.34-216G>T
ENST00000524788.2:n.1026G>T
ENST00000524903.2:n.1142G>T
ENST00000528571.6:c.90-216G>T	ENSP00000434647.1:n.90-216G>T
ENST00000530040.2:n.259-216G>T
ENST00000533371.6:c.-500-216G>T	ENSP00000437066.1:n.-500-216G>T
ENST00000534644.6:n.231-216G>T
ENST00000642892.1:c.-447-216G>T	ENSP00000494165.1:n.-447-216G>T
ENST00000643439.1:c.90-216G>T	ENSP00000495849.1:n.90-216G>T
ENST00000643479.1:n.259-216G>T
ENST00000643516.1:c.117-216G>T
ENST00000644151.1:n.1306G>T
ENST00000644218.1:c.230-216G>T	ENSP00000493574.1:n.230-216G>T
ENST00000644683.1:c.230-216G>T	ENSP00000494085.1:n.230-216G>T
ENST00000644810.1:c.229+784G>T	ENSP00000495895.1:n.229+784G>T
ENST00000644831.1:n.259-216G>T
ENST00000644933.1:c.-500-216G>T	ENSP00000496133.1:n.-500-216G>T
ENST00000645020.1:n.1042G>T
ENST00000645285.1:c.-500-216G>T	ENSP00000495058.1:n.-500-216G>T
ENST00000645331.1:n.252-216G>T
ENST00000645620.1:c.-442-216G>T	ENSP00000493657.1:n.-442-216G>T
ENST00000646777.1:n.259-216G>T
ENST00000647016.1:n.347G>T
ENST00000647152.1:c.-500-216G>T	ENSP00000495893.1:n.-500-216G>T
ENST00000647209.1:c.*99-216G>T	ENSP00000495558.1:n.*99-216G>T
ENST00000647346.1:n.1034G>T
ENST00000299427.10:c.230-216G>T	ENSP00000299427.6:n.230-216G>T
ENST00000428886.6:n.252-216G>T
ENST00000436873.6:c.230-216G>T	ENSP00000398136.2:n.230-216G>T
ENST00000528571.5:c.90-216G>T	ENSP00000434647.1:n.90-216G>T
ENST00000528917.1:n.531-216G>T
ENST00000530040.1:n.342-216G>T
ENST00000533371.5:c.-500-216G>T	ENSP00000437066.1:n.-500-216G>T
ENST00000534644.5:n.215-216G>T
ENST00000611494.4:c.230-216G>T	ENSP00000484546.1:n.230-216G>T
NM_000391.3:c.230-216G>T	NP_000382.3:n.230-216G>T
NM_000391.4:c.230-216G>T MANE Select	NP_000382.3:n.230-216G>T