Canonical Allele Identifier: CA2580083873
Gene: TALDO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2427964
ClinVar RCV Id: RCV003116935

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.763911_763912delinsAA , CM000673.2:g.763911_763912delinsAA GRCh38
NC_000011.9:g.763911_763912delinsAA , CM000673.1:g.763911_763912delinsAA GRCh37
NC_000011.8:g.753911_753912delinsAA NCBI36
NG_008160.1:g.21480_21481delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000319006.8:c.802_803delinsAA MANE Select ENSP00000321259.3:p.Ala268Asn
ENST00000319006.7:c.802_803delinsAA ENSP00000321259.3:p.Ala268Asn
ENST00000528097.5:c.802_803delinsAA ENSP00000437098.1:p.Ala268Asn
NM_006755.1:c.802_803delinsAA NP_006746.1:p.Ala268Asn
NM_006755.2:c.802_803delinsAA MANE Select NP_006746.1:p.Ala268Asn