Canonical Allele Identifier: CA379475144

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638029T>A (hg19) ; chr11:g.6616798T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616798T>A , CM000673.2:g.6616798T>A	GRCh38
NC_000011.9:g.6638029T>A , CM000673.1:g.6638029T>A	GRCh37
NC_000011.8:g.6594605T>A	NCBI36
NG_008653.1:g.7664A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.635A>T	ENSP00000507321.1:p.Asn212Ile
ENST00000299427.12:c.749A>T MANE Select	ENSP00000299427.6:p.Asn250Ile
ENST00000436873.7:c.312+503A>T
ENST00000524788.2:n.1908A>T
ENST00000524903.2:n.2024A>T
ENST00000528807.2:n.405A>T
ENST00000530040.2:n.480-295A>T
ENST00000533371.6:c.20A>T	ENSP00000437066.1:p.Asn7Ile
ENST00000642892.1:c.20A>T	ENSP00000494165.1:p.Asn7Ile
ENST00000643439.1:c.*489A>T	ENSP00000495849.1:n.*489A>T
ENST00000643479.1:n.778A>T
ENST00000643516.1:c.396-295A>T
ENST00000644151.1:n.2188A>T
ENST00000644218.1:c.749A>T	ENSP00000493574.1:p.Asn250Ile
ENST00000644683.1:c.*202A>T	ENSP00000494085.1:n.*202A>T
ENST00000644810.1:c.470A>T	ENSP00000495895.1:p.Asn157Ile
ENST00000644831.1:n.925A>T
ENST00000644933.1:c.20A>T	ENSP00000496133.1:p.Asn7Ile
ENST00000645020.1:n.2039A>T
ENST00000645285.1:c.20A>T	ENSP00000495058.1:p.Asn7Ile
ENST00000645331.1:n.1115A>T
ENST00000645620.1:c.20A>T	ENSP00000493657.1:p.Asn7Ile
ENST00000646777.1:n.925A>T
ENST00000647016.1:n.1229A>T
ENST00000647152.1:c.20A>T	ENSP00000495893.1:p.Asn7Ile
ENST00000647209.1:c.*618A>T	ENSP00000495558.1:n.*618A>T
ENST00000647346.1:n.1769A>T
ENST00000299427.10:c.749A>T	ENSP00000299427.6:p.Asn250Ile
ENST00000436873.6:c.451-295A>T	ENSP00000398136.2:n.451-295A>T
ENST00000524788.1:n.449A>T
ENST00000528807.1:n.299A>T
ENST00000533371.5:c.20A>T	ENSP00000437066.1:p.Asn7Ile
ENST00000611494.4:c.749A>T	ENSP00000484546.1:p.Asn250Ile
NM_000391.3:c.749A>T	NP_000382.3:p.Asn250Ile
NM_000391.4:c.749A>T MANE Select	NP_000382.3:p.Asn250Ile