Canonical Allele Identifier: CA472923046

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6638970C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6617739C>G , CM000673.2:g.6617739C>G	GRCh38
NC_000011.9:g.6638970C>G , CM000673.1:g.6638970C>G	GRCh37
NC_000011.8:g.6595546C>G	NCBI36
NG_008653.1:g.6723G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.153G>C	ENSP00000507321.1:p.Val51=
ENST00000299427.12:c.267G>C MANE Select	ENSP00000299427.6:p.Val89=
ENST00000428886.7:n.355G>C
ENST00000436873.7:c.71G>C
ENST00000524788.2:n.1279G>C
ENST00000524903.2:n.1395G>C
ENST00000528571.6:c.*7G>C	ENSP00000434647.1:n.*7G>C
ENST00000530040.2:n.296G>C
ENST00000533371.6:c.-463G>C	ENSP00000437066.1:n.-463G>C
ENST00000534644.6:n.268G>C
ENST00000642892.1:c.-410G>C	ENSP00000494165.1:n.-410G>C
ENST00000643439.1:c.*7G>C	ENSP00000495849.1:n.*7G>C
ENST00000643479.1:n.296G>C
ENST00000643516.1:c.154G>C
ENST00000644151.1:n.1559G>C
ENST00000644218.1:c.267G>C	ENSP00000493574.1:p.Val89=
ENST00000644683.1:c.267G>C	ENSP00000494085.1:p.Val89=
ENST00000644810.1:c.230-586G>C	ENSP00000495895.1:n.230-586G>C
ENST00000644831.1:n.296G>C
ENST00000644933.1:c.-463G>C	ENSP00000496133.1:n.-463G>C
ENST00000645020.1:n.1295G>C
ENST00000645285.1:c.-463G>C	ENSP00000495058.1:n.-463G>C
ENST00000645331.1:n.289G>C
ENST00000645620.1:c.-405G>C	ENSP00000493657.1:n.-405G>C
ENST00000646777.1:n.296G>C
ENST00000647016.1:n.600G>C
ENST00000647152.1:c.-463G>C	ENSP00000495893.1:n.-463G>C
ENST00000647209.1:c.*136G>C	ENSP00000495558.1:n.*136G>C
ENST00000647346.1:n.1287G>C
ENST00000299427.10:c.267G>C	ENSP00000299427.6:p.Val89=
ENST00000428886.6:n.289G>C
ENST00000436873.6:c.267G>C	ENSP00000398136.2:p.Val89=
ENST00000528571.5:c.*7G>C	ENSP00000434647.1:n.*7G>C
ENST00000530040.1:n.379G>C
ENST00000533371.5:c.-463G>C	ENSP00000437066.1:n.-463G>C
ENST00000534644.5:n.252G>C
ENST00000611494.4:c.267G>C	ENSP00000484546.1:p.Val89=
NM_000391.3:c.267G>C	NP_000382.3:p.Val89=
NM_000391.4:c.267G>C MANE Select	NP_000382.3:p.Val89=