Canonical Allele Identifier: CA378934539
Gene: TALDO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2575047
ClinVar RCV Id: RCV003319944
dbSNP Id: rs1279835702
gnomAD v2: 11-763394-C-T
gnomAD v3: 11-763394-C-T
gnomAD v4: 11-763394-C-T
MyVariant Identifiers: chr11:g.763394C>T (hg19) chr11:g.763394C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.763394C>T , CM000673.2:g.763394C>T GRCh38
NC_000011.9:g.763394C>T , CM000673.1:g.763394C>T GRCh37
NC_000011.8:g.753394C>T NCBI36
NG_008160.1:g.20963C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000319006.8:c.512C>T MANE Select ENSP00000321259.3:p.Ser171Phe
ENST00000319006.7:c.512C>T ENSP00000321259.3:p.Ser171Phe
ENST00000528070.5:c.*510C>T ENSP00000435042.1:n.*510C>T
ENST00000528097.5:c.512C>T ENSP00000437098.1:p.Ser171Phe
ENST00000530440.1:c.*171C>T ENSP00000433501.1:n.*171C>T
NM_006755.1:c.512C>T NP_006746.1:p.Ser171Phe
NM_006755.2:c.512C>T MANE Select NP_006746.1:p.Ser171Phe
Search 100 bp 5'
Search 100 bp 3'