Canonical Allele Identifier: CA2279749852
Gene: TYMS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.662151C= , CM000680.2:g.662151C= GRCh38
NC_000018.9:g.662151C= , CM000680.1:g.662151C= GRCh37
NC_000018.8:g.652151C= NCBI36
NG_028255.1:g.9548C= , LRG_783:g.9548C=

Transcript Alleles

HGVS Amino-acid change
ENST00000323274.15:c.285C= MANE Select ENSP00000315644.10:p.Ser95=
ENST00000323224.7:c.285C= ENSP00000314727.7:p.Ser95=
ENST00000323250.9:c.205+4204C= ENSP00000314902.5:n.205+4204C=
ENST00000323274.14:c.285C= ENSP00000315644.10:p.Ser95=
ENST00000579128.1:n.363C=
NM_001071.2:c.285C= , LRG_783t1:c.285C= NP_001062.1:p.Ser95=
NM_001071.3:c.285C= NP_001062.1:p.Ser95=
NM_001354867.1:c.285C= NP_001341796.1:p.Ser95=
NM_001354868.1:c.205+4204C= NP_001341797.1:n.205+4204C=
NM_001071.4:c.285C= MANE Select NP_001062.1:p.Ser95=
NM_001354867.2:c.285C= NP_001341796.1:p.Ser95=
NM_001354868.2:c.205+4204C= NP_001341797.1:n.205+4204C=