Canonical Allele Identifier: CA2551521476

Gene: TYMS

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.661994_661997del , CM000680.2:g.661994_661997del	GRCh38
NC_000018.9:g.661994_661997del , CM000680.1:g.661994_661997del	GRCh37
NC_000018.8:g.651994_651997del	NCBI36
NG_028255.1:g.9391_9394del , LRG_783:g.9391_9394del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323274.15:c.280-152_280-149del MANE Select	ENSP00000315644.10:n.280-152_280-149del
ENST00000323224.7:c.280-152_280-149del	ENSP00000314727.7:n.280-152_280-149del
ENST00000323250.9:c.205+4047_205+4050del	ENSP00000314902.5:n.205+4047_205+4050del
ENST00000323274.14:c.280-152_280-149del	ENSP00000315644.10:n.280-152_280-149del
ENST00000579128.1:n.358-152_358-149del
NM_001071.2:c.280-152_280-149del , LRG_783t1:c.280-152_280-149del	NP_001062.1:n.280-152_280-149del
NM_001071.3:c.280-152_280-149del	NP_001062.1:n.280-152_280-149del
NM_001354867.1:c.280-152_280-149del	NP_001341796.1:n.280-152_280-149del
NM_001354868.1:c.205+4047_205+4050del	NP_001341797.1:n.205+4047_205+4050del
NM_001071.4:c.280-152_280-149del MANE Select	NP_001062.1:n.280-152_280-149del
NM_001354867.2:c.280-152_280-149del	NP_001341796.1:n.280-152_280-149del
NM_001354868.2:c.205+4047_205+4050del	NP_001341797.1:n.205+4047_205+4050del