Canonical Allele Identifier: CA379474989

Gene: TPP1

Linked Data

• MyVariant Identifiers: chr11:g.6637948A>G (hg19) ; chr11:g.6616717A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616717A>G , CM000673.2:g.6616717A>G	GRCh38
NC_000011.9:g.6637948A>G , CM000673.1:g.6637948A>G	GRCh37
NC_000011.8:g.6594524A>G	NCBI36
NG_008653.1:g.7745T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.716T>C	ENSP00000507321.1:p.Val239Ala
ENST00000299427.12:c.830T>C MANE Select	ENSP00000299427.6:p.Val277Ala
ENST00000436873.7:c.312+584T>C
ENST00000524788.2:n.1989T>C
ENST00000524903.2:n.2105T>C
ENST00000528807.2:n.486T>C
ENST00000530040.2:n.480-214T>C
ENST00000533371.6:c.101T>C	ENSP00000437066.1:p.Val34Ala
ENST00000642892.1:c.101T>C	ENSP00000494165.1:p.Val34Ala
ENST00000643439.1:c.*570T>C	ENSP00000495849.1:n.*570T>C
ENST00000643479.1:n.859T>C
ENST00000643516.1:c.396-214T>C
ENST00000644151.1:n.2269T>C
ENST00000644218.1:c.830T>C	ENSP00000493574.1:p.Val277Ala
ENST00000644683.1:c.*283T>C	ENSP00000494085.1:n.*283T>C
ENST00000644810.1:c.551T>C	ENSP00000495895.1:p.Val184Ala
ENST00000644831.1:n.1006T>C
ENST00000644933.1:c.101T>C	ENSP00000496133.1:p.Val34Ala
ENST00000645020.1:n.2120T>C
ENST00000645285.1:c.101T>C	ENSP00000495058.1:p.Val34Ala
ENST00000645331.1:n.1196T>C
ENST00000645620.1:c.101T>C	ENSP00000493657.1:p.Val34Ala
ENST00000646777.1:n.1006T>C
ENST00000647016.1:n.1310T>C
ENST00000647152.1:c.101T>C	ENSP00000495893.1:p.Val34Ala
ENST00000647209.1:c.*699T>C	ENSP00000495558.1:n.*699T>C
ENST00000647346.1:n.1850T>C
ENST00000299427.10:c.830T>C	ENSP00000299427.6:p.Val277Ala
ENST00000436873.6:c.451-214T>C	ENSP00000398136.2:n.451-214T>C
ENST00000524788.1:n.530T>C
ENST00000528807.1:n.380T>C
ENST00000533371.5:c.101T>C	ENSP00000437066.1:p.Val34Ala
ENST00000611494.4:c.830T>C	ENSP00000484546.1:p.Val277Ala
NM_000391.3:c.830T>C	NP_000382.3:p.Val277Ala
NM_000391.4:c.830T>C MANE Select	NP_000382.3:p.Val277Ala