Canonical Allele Identifier: CA2279749794
Gene: TYMS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.662051G= , CM000680.2:g.662051G= GRCh38
NC_000018.9:g.662051G= , CM000680.1:g.662051G= GRCh37
NC_000018.8:g.652051G= NCBI36
NG_028255.1:g.9448G= , LRG_783:g.9448G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323274.15:c.280-95G= MANE Select ENSP00000315644.10:n.280-95G=
ENST00000323224.7:c.280-95G= ENSP00000314727.7:n.280-95G=
ENST00000323250.9:c.205+4104G= ENSP00000314902.5:n.205+4104G=
ENST00000323274.14:c.280-95G= ENSP00000315644.10:n.280-95G=
ENST00000579128.1:n.358-95G=
NM_001071.2:c.280-95G= , LRG_783t1:c.280-95G= NP_001062.1:n.280-95G=
NM_001071.3:c.280-95G= NP_001062.1:n.280-95G=
NM_001354867.1:c.280-95G= NP_001341796.1:n.280-95G=
NM_001354868.1:c.205+4104G= NP_001341797.1:n.205+4104G=
NM_001071.4:c.280-95G= MANE Select NP_001062.1:n.280-95G=
NM_001354867.2:c.280-95G= NP_001341796.1:n.280-95G=
NM_001354868.2:c.205+4104G= NP_001341797.1:n.205+4104G=