Canonical Allele Identifier: CA597439644

Gene: TPP1

Linked Data

• dbSNP Id: rs1201457949
• gnomAD v2: 11-6637737-GGAT-G
• gnomAD v4: 11-6616506-GGAT-G
• MyVariant Identifiers: chr11:g.6637738_6637740del (hg19) ; chr11:g.6616507_6616509del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616507_6616509del , CM000673.2:g.6616507_6616509del	GRCh38
NC_000011.9:g.6637738_6637740del , CM000673.1:g.6637738_6637740del	GRCh37
NC_000011.8:g.6594314_6594316del	NCBI36
NG_008653.1:g.7953_7955del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682424.1:c.773-6_773-4del	ENSP00000507321.1:n.773-6_773-4del
ENST00000299427.12:c.887-6_887-4del MANE Select	ENSP00000299427.6:n.887-6_887-4del
ENST00000436873.7:c.313-435_313-433del
ENST00000530040.2:n.480-6_480-4del
ENST00000533371.6:c.158-6_158-4del	ENSP00000437066.1:n.158-6_158-4del
ENST00000642892.1:c.158-6_158-4del	ENSP00000494165.1:n.158-6_158-4del
ENST00000643439.1:c.*627-6_*627-4del	ENSP00000495849.1:n.*627-6_*627-4del
ENST00000643479.1:n.1067_1069del
ENST00000643516.1:c.396-6_396-4del
ENST00000644218.1:c.886+152_886+154del	ENSP00000493574.1:n.886+152_886+154del
ENST00000644683.1:c.*340-6_*340-4del	ENSP00000494085.1:n.*340-6_*340-4del
ENST00000644810.1:c.608-6_608-4del	ENSP00000495895.1:n.608-6_608-4del
ENST00000644831.1:n.1063-6_1063-4del
ENST00000644933.1:c.158-6_158-4del	ENSP00000496133.1:n.158-6_158-4del
ENST00000645285.1:c.157+152_157+154del	ENSP00000495058.1:n.157+152_157+154del
ENST00000645331.1:n.1404_1406del
ENST00000645620.1:c.158-6_158-4del	ENSP00000493657.1:n.158-6_158-4del
ENST00000646777.1:n.1214_1216del
ENST00000647016.1:n.1367-6_1367-4del
ENST00000647152.1:c.158-6_158-4del	ENSP00000495893.1:n.158-6_158-4del
ENST00000647209.1:c.*756-6_*756-4del	ENSP00000495558.1:n.*756-6_*756-4del
ENST00000647346.1:n.1907-6_1907-4del
ENST00000299427.10:c.887-6_887-4del	ENSP00000299427.6:n.887-6_887-4del
ENST00000436873.6:c.451-6_451-4del	ENSP00000398136.2:n.451-6_451-4del
ENST00000533371.5:c.158-6_158-4del	ENSP00000437066.1:n.158-6_158-4del
ENST00000611494.4:c.887-6_887-4del	ENSP00000484546.1:n.887-6_887-4del
NM_000391.3:c.887-6_887-4del	NP_000382.3:n.887-6_887-4del
NM_000391.4:c.887-6_887-4del MANE Select	NP_000382.3:n.887-6_887-4del