Canonical Allele Identifier: CA781538359

Gene: TYMS

Linked Data

• dbSNP Id: rs1165265024
• gnomAD v3: 18-662030-ACCT-A
• gnomAD v4: 18-662030-ACCT-A
• MyVariant Identifiers: chr18:g.662031_662033del (hg19) ; chr18:g.662031_662033del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.662034_662036del , CM000680.2:g.662034_662036del	GRCh38
NC_000018.9:g.662034_662036del , CM000680.1:g.662034_662036del	GRCh37
NC_000018.8:g.652034_652036del	NCBI36
NG_028255.1:g.9431_9433del , LRG_783:g.9431_9433del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323274.15:c.280-112_280-110del MANE Select	ENSP00000315644.10:n.280-112_280-110del
ENST00000323224.7:c.280-112_280-110del	ENSP00000314727.7:n.280-112_280-110del
ENST00000323250.9:c.205+4087_205+4089del	ENSP00000314902.5:n.205+4087_205+4089del
ENST00000323274.14:c.280-112_280-110del	ENSP00000315644.10:n.280-112_280-110del
ENST00000579128.1:n.358-112_358-110del
NM_001071.2:c.280-112_280-110del , LRG_783t1:c.280-112_280-110del	NP_001062.1:n.280-112_280-110del
NM_001071.3:c.280-112_280-110del	NP_001062.1:n.280-112_280-110del
NM_001354867.1:c.280-112_280-110del	NP_001341796.1:n.280-112_280-110del
NM_001354868.1:c.205+4087_205+4089del	NP_001341797.1:n.205+4087_205+4089del
NM_001071.4:c.280-112_280-110del MANE Select	NP_001062.1:n.280-112_280-110del
NM_001354867.2:c.280-112_280-110del	NP_001341796.1:n.280-112_280-110del
NM_001354868.2:c.205+4087_205+4089del	NP_001341797.1:n.205+4087_205+4089del