Canonical Allele Identifier: CA401670013
Gene: TYMS HGNC NCBI

Linked Data

gnomAD v4: 18-662177-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.662177A>G , CM000680.2:g.662177A>G GRCh38
NC_000018.9:g.662177A>G , CM000680.1:g.662177A>G GRCh37
NC_000018.8:g.652177A>G NCBI36
NG_028255.1:g.9574A>G , LRG_783:g.9574A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323274.15:c.311A>G MANE Select ENSP00000315644.10:p.Lys104Arg
ENST00000323224.7:c.311A>G ENSP00000314727.7:p.Lys104Arg
ENST00000323250.9:c.205+4230A>G ENSP00000314902.5:n.205+4230A>G
ENST00000323274.14:c.311A>G ENSP00000315644.10:p.Lys104Arg
ENST00000579128.1:n.389A>G
NM_001071.2:c.311A>G , LRG_783t1:c.311A>G NP_001062.1:p.Lys104Arg
NM_001071.3:c.311A>G NP_001062.1:p.Lys104Arg
NM_001354867.1:c.311A>G NP_001341796.1:p.Lys104Arg
NM_001354868.1:c.205+4230A>G NP_001341797.1:n.205+4230A>G
NM_001071.4:c.311A>G MANE Select NP_001062.1:p.Lys104Arg
NM_001354867.2:c.311A>G NP_001341796.1:p.Lys104Arg
NM_001354868.2:c.205+4230A>G NP_001341797.1:n.205+4230A>G