Canonical Allele Identifier: CA5788293
Gene: TALDO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2185021
ClinVar RCV Id: RCV002603609
dbSNP Id: rs138088112
ExAC: 11:763911 G / A
gnomAD v2: 11-763911-G-A
gnomAD v3: 11-763911-G-A
gnomAD v4: 11-763911-G-A
MyVariant Identifiers: chr11:g.763911G>A (hg19) chr11:g.763911G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.763911G>A , CM000673.2:g.763911G>A GRCh38
NC_000011.9:g.763911G>A , CM000673.1:g.763911G>A GRCh37
NC_000011.8:g.753911G>A NCBI36
NG_008160.1:g.21480G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319006.8:c.802G>A MANE Select ENSP00000321259.3:p.Ala268Thr
ENST00000319006.7:c.802G>A ENSP00000321259.3:p.Ala268Thr
ENST00000528097.5:c.802G>A ENSP00000437098.1:p.Ala268Thr
NM_006755.1:c.802G>A NP_006746.1:p.Ala268Thr
NM_006755.2:c.802G>A MANE Select NP_006746.1:p.Ala268Thr
Search 100 bp 5'
Search 100 bp 3'