Canonical Allele Identifier: CA472334222
Gene: TALDO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.763395C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.763395C>T , CM000673.2:g.763395C>T GRCh38
NC_000011.9:g.763395C>T , CM000673.1:g.763395C>T GRCh37
NC_000011.8:g.753395C>T NCBI36
NG_008160.1:g.20964C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000319006.8:c.513C>T MANE Select ENSP00000321259.3:p.Ser171=
ENST00000319006.7:c.513C>T ENSP00000321259.3:p.Ser171=
ENST00000528070.5:c.*511C>T ENSP00000435042.1:n.*511C>T
ENST00000528097.5:c.513C>T ENSP00000437098.1:p.Ser171=
ENST00000530440.1:c.*172C>T ENSP00000433501.1:n.*172C>T
NM_006755.1:c.513C>T NP_006746.1:p.Ser171=
NM_006755.2:c.513C>T MANE Select NP_006746.1:p.Ser171=
Search 100 bp 5'
Search 100 bp 3'