Canonical Allele Identifier: CA378937560
Gene: TALDO1 HGNC NCBI

Linked Data

dbSNP Id: rs1863002339
gnomAD v3: 11-763906-A-C
gnomAD v4: 11-763906-A-C
MyVariant Identifiers: chr11:g.763906A>C (hg19) chr11:g.763906A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.763906A>C , CM000673.2:g.763906A>C GRCh38
NC_000011.9:g.763906A>C , CM000673.1:g.763906A>C GRCh37
NC_000011.8:g.753906A>C NCBI36
NG_008160.1:g.21475A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000319006.8:c.797A>C MANE Select ENSP00000321259.3:p.Asp266Ala
ENST00000319006.7:c.797A>C ENSP00000321259.3:p.Asp266Ala
ENST00000528097.5:c.797A>C ENSP00000437098.1:p.Asp266Ala
NM_006755.1:c.797A>C NP_006746.1:p.Asp266Ala
NM_006755.2:c.797A>C MANE Select NP_006746.1:p.Asp266Ala
Search 100 bp 5'
Search 100 bp 3'