Canonical Allele Identifier: CA401669878
Gene: TYMS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.662153C>T , CM000680.2:g.662153C>T GRCh38
NC_000018.9:g.662153C>T , CM000680.1:g.662153C>T GRCh37
NC_000018.8:g.652153C>T NCBI36
NG_028255.1:g.9550C>T , LRG_783:g.9550C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000323274.15:c.287C>T MANE Select ENSP00000315644.10:p.Thr96Ile
ENST00000323224.7:c.287C>T ENSP00000314727.7:p.Thr96Ile
ENST00000323250.9:c.205+4206C>T ENSP00000314902.5:n.205+4206C>T
ENST00000323274.14:c.287C>T ENSP00000315644.10:p.Thr96Ile
ENST00000579128.1:n.365C>T
NM_001071.2:c.287C>T , LRG_783t1:c.287C>T NP_001062.1:p.Thr96Ile
NM_001071.3:c.287C>T NP_001062.1:p.Thr96Ile
NM_001354867.1:c.287C>T NP_001341796.1:p.Thr96Ile
NM_001354868.1:c.205+4206C>T NP_001341797.1:n.205+4206C>T
NM_001071.4:c.287C>T MANE Select NP_001062.1:p.Thr96Ile
NM_001354867.2:c.287C>T NP_001341796.1:p.Thr96Ile
NM_001354868.2:c.205+4206C>T NP_001341797.1:n.205+4206C>T