Canonical Allele Identifier: CA597439878

Gene: TPP1

Linked Data

• gnomAD v2: 11-6636559-TCCTGAAAGGCATTTTTGAGTGAGTATTGGCATGTGGCCTGCCCAGCAGTCAGCTGAACTGAGGATCCCCCATCCTCACTCTTACCCTGCATCCATCCACACAAACACACGTA-T
• MyVariant Identifiers: chr11:g.6636560_6636671del (hg19) ; chr11:g.6615329_6615440del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6615333_6615444del , CM000673.2:g.6615333_6615444del	GRCh38
NC_000011.9:g.6636564_6636675del , CM000673.1:g.6636564_6636675del	GRCh37
NC_000011.8:g.6593140_6593251del	NCBI36
NG_008653.1:g.9022_9133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.1152+2_1153del
ENST00000299427.12:c.1266+2_1267del
ENST00000436873.7:c.503+2_504del
ENST00000524611.2:n.16_127del
ENST00000524924.2:n.386+2_387del
ENST00000533371.6:c.537+2_538del
ENST00000642892.1:c.537+2_538del
ENST00000643342.1:c.339+2_340del
ENST00000643439.1:c.*1006+2_*1007del
ENST00000643479.1:n.1452+2_1453del
ENST00000643516.1:c.775+2_776del
ENST00000644218.1:c.1077+2_1078del
ENST00000644683.1:c.*719+2_*720del
ENST00000644810.1:c.987+2_988del
ENST00000644831.1:n.1442+2_1443del
ENST00000644933.1:c.*132+2_*133del
ENST00000645285.1:c.*132+2_*133del
ENST00000645331.1:n.2471+2_2472del
ENST00000645620.1:c.537+2_538del
ENST00000646691.1:n.1043_1154del
ENST00000646777.1:n.1599+2_1600del
ENST00000647016.1:n.1746+2_1747del
ENST00000647152.1:c.537+2_538del
ENST00000647209.1:c.*1135+2_*1136del
ENST00000647346.1:n.2286+2_2287del
ENST00000299427.10:c.1266+2_1267del
ENST00000524611.1:n.34_145del
ENST00000524924.1:n.221+2_222del
ENST00000532191.1:n.319+2_320del
ENST00000533371.5:c.537+2_538del
ENST00000611494.4:c.1266+2_1267del
NM_000391.3:c.1266+2_1267del
NM_000391.4:c.1266+2_1267del