Canonical Allele Identifier: CA2279749785
Gene: TYMS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.662033T= , CM000680.2:g.662033T= GRCh38
NC_000018.9:g.662033T= , CM000680.1:g.662033T= GRCh37
NC_000018.8:g.652033T= NCBI36
NG_028255.1:g.9430T= , LRG_783:g.9430T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323274.15:c.280-113T= MANE Select ENSP00000315644.10:n.280-113T=
ENST00000323224.7:c.280-113T= ENSP00000314727.7:n.280-113T=
ENST00000323250.9:c.205+4086T= ENSP00000314902.5:n.205+4086T=
ENST00000323274.14:c.280-113T= ENSP00000315644.10:n.280-113T=
ENST00000579128.1:n.358-113T=
NM_001071.2:c.280-113T= , LRG_783t1:c.280-113T= NP_001062.1:n.280-113T=
NM_001071.3:c.280-113T= NP_001062.1:n.280-113T=
NM_001354867.1:c.280-113T= NP_001341796.1:n.280-113T=
NM_001354868.1:c.205+4086T= NP_001341797.1:n.205+4086T=
NM_001071.4:c.280-113T= MANE Select NP_001062.1:n.280-113T=
NM_001354867.2:c.280-113T= NP_001341796.1:n.280-113T=
NM_001354868.2:c.205+4086T= NP_001341797.1:n.205+4086T=