Canonical Allele Identifier: CA379474923

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6637922T>C (hg19) ; chr11:g.6616691T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616691T>C , CM000673.2:g.6616691T>C	GRCh38
NC_000011.9:g.6637922T>C , CM000673.1:g.6637922T>C	GRCh37
NC_000011.8:g.6594498T>C	NCBI36
NG_008653.1:g.7771A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.742A>G	ENSP00000507321.1:p.Asn248Asp
ENST00000299427.12:c.856A>G MANE Select	ENSP00000299427.6:p.Asn286Asp
ENST00000436873.7:c.312+610A>G
ENST00000524788.2:n.2015A>G
ENST00000524903.2:n.2131A>G
ENST00000528807.2:n.512A>G
ENST00000530040.2:n.480-188A>G
ENST00000533371.6:c.127A>G	ENSP00000437066.1:p.Asn43Asp
ENST00000642892.1:c.127A>G	ENSP00000494165.1:p.Asn43Asp
ENST00000643439.1:c.*596A>G	ENSP00000495849.1:n.*596A>G
ENST00000643479.1:n.885A>G
ENST00000643516.1:c.396-188A>G
ENST00000644151.1:n.2295A>G
ENST00000644218.1:c.856A>G	ENSP00000493574.1:p.Asn286Asp
ENST00000644683.1:c.*309A>G	ENSP00000494085.1:n.*309A>G
ENST00000644810.1:c.577A>G	ENSP00000495895.1:p.Asn193Asp
ENST00000644831.1:n.1032A>G
ENST00000644933.1:c.127A>G	ENSP00000496133.1:p.Asn43Asp
ENST00000645020.1:n.2146A>G
ENST00000645285.1:c.127A>G	ENSP00000495058.1:p.Asn43Asp
ENST00000645331.1:n.1222A>G
ENST00000645620.1:c.127A>G	ENSP00000493657.1:p.Asn43Asp
ENST00000646777.1:n.1032A>G
ENST00000647016.1:n.1336A>G
ENST00000647152.1:c.127A>G	ENSP00000495893.1:p.Asn43Asp
ENST00000647209.1:c.*725A>G	ENSP00000495558.1:n.*725A>G
ENST00000647346.1:n.1876A>G
ENST00000299427.10:c.856A>G	ENSP00000299427.6:p.Asn286Asp
ENST00000436873.6:c.451-188A>G	ENSP00000398136.2:n.451-188A>G
ENST00000528807.1:n.406A>G
ENST00000533371.5:c.127A>G	ENSP00000437066.1:p.Asn43Asp
ENST00000611494.4:c.856A>G	ENSP00000484546.1:p.Asn286Asp
NM_000391.3:c.856A>G	NP_000382.3:p.Asn286Asp
NM_000391.4:c.856A>G MANE Select	NP_000382.3:p.Asn286Asp