Canonical Allele Identifier: CA2576440785
Gene: TYMS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.662249_662251del , CM000680.2:g.662249_662251del GRCh38
NC_000018.9:g.662249_662251del , CM000680.1:g.662249_662251del GRCh37
NC_000018.8:g.652249_652251del NCBI36
NG_028255.1:g.9646_9648del , LRG_783:g.9646_9648del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323274.15:c.383_385del MANE Select ENSP00000315644.10:p.Glu128del
ENST00000323224.7:c.383_385del ENSP00000314727.7:p.Glu128del
ENST00000323250.9:c.205+4302_205+4304del ENSP00000314902.5:n.205+4302_205+4304del
ENST00000323274.14:c.383_385del ENSP00000315644.10:p.Glu128del
ENST00000579128.1:n.461_463del
NM_001071.2:c.383_385del , LRG_783t1:c.383_385del NP_001062.1:p.Glu128del
NM_001071.3:c.383_385del NP_001062.1:p.Glu128del
NM_001354867.1:c.383_385del NP_001341796.1:p.Glu128del
NM_001354868.1:c.205+4302_205+4304del NP_001341797.1:n.205+4302_205+4304del
NM_001071.4:c.383_385del MANE Select NP_001062.1:p.Glu128del
NM_001354867.2:c.383_385del NP_001341796.1:p.Glu128del
NM_001354868.2:c.205+4302_205+4304del NP_001341797.1:n.205+4302_205+4304del