Canonical Allele Identifier: CA597021701
Gene: TALDO1 HGNC NCBI

Linked Data

dbSNP Id: rs1564993927
gnomAD v2: 11-763182-TTCACCTGCCCCGCCCTCACCTGCCCCGCCCTCACCTGCCCCCGCCCTCACCCGCCCCCGCCCTCACCCATCCCCGCCCTCACCGTCCCCGCCCTCACCCGCCCCCGCCCTCACCTGTCCCCGCCC-T
gnomAD v3: 11-763182-TTCACCTGCCCCGCCCTCACCTGCCCCGCCCTCACCTGCCCCCGCCCTCACCCGCCCCCGCCCTCACCCATCCCCGCCCTCACCGTCCCCGCCCTCACCCGCCCCCGCCCTCACCTGTCCCCGCCC-T
gnomAD v4: 11-763182-TTCACCTGCCCCGCCCTCACCTGCCCCGCCCTCACCTGCCCCCGCCCTCACCCGCCCCCGCCCTCACCCATCCCCGCCCTCACCGTCCCCGCCCTCACCCGCCCCCGCCCTCACCTGTCCCCGCCC-T
MyVariant Identifiers: chr11:g.763183_763307del (hg19) chr11:g.763183_763307del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.763205_763329del , CM000673.2:g.763205_763329del GRCh38
NC_000011.9:g.763205_763329del , CM000673.1:g.763205_763329del GRCh37
NC_000011.8:g.753205_753329del NCBI36
NG_008160.1:g.20774_20898del

Transcript Alleles

HGVS Amino-acid change
ENST00000319006.8:c.462-139_462-15del MANE Select ENSP00000321259.3:n.462-139_462-15del
ENST00000319006.7:c.462-139_462-15del ENSP00000321259.3:n.462-139_462-15del
ENST00000528070.5:c.*460-139_*460-15del ENSP00000435042.1:n.*460-139_*460-15del
ENST00000528097.5:c.462-139_462-15del ENSP00000437098.1:n.462-139_462-15del
ENST00000530440.1:c.*121-139_*121-15del ENSP00000433501.1:n.*121-139_*121-15del
NM_006755.1:c.462-139_462-15del NP_006746.1:n.462-139_462-15del
NM_006755.2:c.462-139_462-15del MANE Select NP_006746.1:n.462-139_462-15del
Search 100 bp 5'
Search 100 bp 3'