Canonical Allele Identifier: CA934783772

Gene: TPP1

Linked Data

• gnomAD v3: 11-6616536-G-GTTT
• gnomAD v4: 11-6616536-G-GTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616536_6616537insTTT , CM000673.2:g.6616536_6616537insTTT	GRCh38
NC_000011.9:g.6637767_6637768insTTT , CM000673.1:g.6637767_6637768insTTT	GRCh37
NC_000011.8:g.6594343_6594344insTTT	NCBI36
NG_008653.1:g.7925_7926insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.773-34_773-33insAAA	ENSP00000507321.1:n.773-34_773-33insAAA
ENST00000299427.12:c.887-34_887-33insAAA MANE Select	ENSP00000299427.6:n.887-34_887-33insAAA
ENST00000436873.7:c.313-463_313-462insAAA
ENST00000524903.2:n.2285_2286insAAA
ENST00000530040.2:n.480-34_480-33insAAA
ENST00000533371.6:c.158-34_158-33insAAA	ENSP00000437066.1:n.158-34_158-33insAAA
ENST00000642892.1:c.158-34_158-33insAAA	ENSP00000494165.1:n.158-34_158-33insAAA
ENST00000643439.1:c.*627-34_*627-33insAAA	ENSP00000495849.1:n.*627-34_*627-33insAAA
ENST00000643479.1:n.1039_1040insAAA
ENST00000643516.1:c.396-34_396-33insAAA
ENST00000644218.1:c.886+124_886+125insAAA	ENSP00000493574.1:n.886+124_886+125insAAA
ENST00000644683.1:c.*340-34_*340-33insAAA	ENSP00000494085.1:n.*340-34_*340-33insAAA
ENST00000644810.1:c.608-34_608-33insAAA	ENSP00000495895.1:n.608-34_608-33insAAA
ENST00000644831.1:n.1063-34_1063-33insAAA
ENST00000644933.1:c.158-34_158-33insAAA	ENSP00000496133.1:n.158-34_158-33insAAA
ENST00000645285.1:c.157+124_157+125insAAA	ENSP00000495058.1:n.157+124_157+125insAAA
ENST00000645331.1:n.1376_1377insAAA
ENST00000645620.1:c.158-34_158-33insAAA	ENSP00000493657.1:n.158-34_158-33insAAA
ENST00000646777.1:n.1186_1187insAAA
ENST00000647016.1:n.1367-34_1367-33insAAA
ENST00000647152.1:c.158-34_158-33insAAA	ENSP00000495893.1:n.158-34_158-33insAAA
ENST00000647209.1:c.*756-34_*756-33insAAA	ENSP00000495558.1:n.*756-34_*756-33insAAA
ENST00000647346.1:n.1907-34_1907-33insAAA
ENST00000299427.10:c.887-34_887-33insAAA	ENSP00000299427.6:n.887-34_887-33insAAA
ENST00000436873.6:c.451-34_451-33insAAA	ENSP00000398136.2:n.451-34_451-33insAAA
ENST00000528807.1:n.560_561insAAA
ENST00000533371.5:c.158-34_158-33insAAA	ENSP00000437066.1:n.158-34_158-33insAAA
ENST00000611494.4:c.887-34_887-33insAAA	ENSP00000484546.1:n.887-34_887-33insAAA
NM_000391.3:c.887-34_887-33insAAA	NP_000382.3:n.887-34_887-33insAAA
NM_000391.4:c.887-34_887-33insAAA MANE Select	NP_000382.3:n.887-34_887-33insAAA