Canonical Allele Identifier: CA295418318

Gene: TYMS

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.659829A>T , CM000680.2:g.659829A>T	GRCh38
NC_000018.9:g.659829A>T , CM000680.1:g.659829A>T	GRCh37
NC_000018.8:g.649829A>T	NCBI36
NG_028255.1:g.7226A>T , LRG_783:g.7226A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323274.15:c.279+115A>T MANE Select	ENSP00000315644.10:n.279+115A>T
ENST00000323224.7:c.279+115A>T	ENSP00000314727.7:n.279+115A>T
ENST00000323250.9:c.205+1882A>T	ENSP00000314902.5:n.205+1882A>T
ENST00000323274.14:c.279+115A>T	ENSP00000315644.10:n.279+115A>T
ENST00000579128.1:n.357+115A>T
NM_001071.2:c.279+115A>T , LRG_783t1:c.279+115A>T	NP_001062.1:n.279+115A>T
NM_001071.3:c.279+115A>T	NP_001062.1:n.279+115A>T
NM_001354867.1:c.279+115A>T	NP_001341796.1:n.279+115A>T
NM_001354868.1:c.205+1882A>T	NP_001341797.1:n.205+1882A>T
NM_001071.4:c.279+115A>T MANE Select	NP_001062.1:n.279+115A>T
NM_001354867.2:c.279+115A>T	NP_001341796.1:n.279+115A>T
NM_001354868.2:c.205+1882A>T	NP_001341797.1:n.205+1882A>T