Canonical Allele Identifier: CA2279749862

Gene: TYMS

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.662209C= , CM000680.2:g.662209C=	GRCh38
NC_000018.9:g.662209C= , CM000680.1:g.662209C=	GRCh37
NC_000018.8:g.652209C=	NCBI36
NG_028255.1:g.9606C= , LRG_783:g.9606C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323274.15:c.343C= MANE Select	ENSP00000315644.10:p.Arg115=
ENST00000323224.7:c.343C=	ENSP00000314727.7:p.Arg115=
ENST00000323250.9:c.205+4262C=	ENSP00000314902.5:n.205+4262C=
ENST00000323274.14:c.343C=	ENSP00000315644.10:p.Arg115=
ENST00000579128.1:n.421C=
NM_001071.2:c.343C= , LRG_783t1:c.343C=	NP_001062.1:p.Arg115=
NM_001071.3:c.343C=	NP_001062.1:p.Arg115=
NM_001354867.1:c.343C=	NP_001341796.1:p.Arg115=
NM_001354868.1:c.205+4262C=	NP_001341797.1:n.205+4262C=
NM_001071.4:c.343C= MANE Select	NP_001062.1:p.Arg115=
NM_001354867.2:c.343C=	NP_001341796.1:p.Arg115=
NM_001354868.2:c.205+4262C=	NP_001341797.1:n.205+4262C=