Canonical Allele Identifier: CA472334566
Gene: TALDO1 HGNC NCBI

Linked Data

dbSNP Id: rs1863001737
gnomAD v4: 11-763880-C-T
MyVariant Identifiers: chr11:g.763880C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.763880C>T , CM000673.2:g.763880C>T GRCh38
NC_000011.9:g.763880C>T , CM000673.1:g.763880C>T GRCh37
NC_000011.8:g.753880C>T NCBI36
NG_008160.1:g.21449C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000319006.8:c.771C>T MANE Select ENSP00000321259.3:p.Pro257=
ENST00000319006.7:c.771C>T ENSP00000321259.3:p.Pro257=
ENST00000528097.5:c.771C>T ENSP00000437098.1:p.Pro257=
NM_006755.1:c.771C>T NP_006746.1:p.Pro257=
NM_006755.2:c.771C>T MANE Select NP_006746.1:p.Pro257=
Search 100 bp 5'
Search 100 bp 3'