Canonical Allele Identifier: CA987074715

Gene: TYMS

Linked Data

• dbSNP Id: rs2074760467
• gnomAD v3: 18-661976-ACT-A
• gnomAD v4: 18-661976-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.661980_661981del , CM000680.2:g.661980_661981del	GRCh38
NC_000018.9:g.661980_661981del , CM000680.1:g.661980_661981del	GRCh37
NC_000018.8:g.651980_651981del	NCBI36
NG_028255.1:g.9377_9378del , LRG_783:g.9377_9378del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323274.15:c.280-166_280-165del MANE Select	ENSP00000315644.10:n.280-166_280-165del
ENST00000323224.7:c.280-166_280-165del	ENSP00000314727.7:n.280-166_280-165del
ENST00000323250.9:c.205+4033_205+4034del	ENSP00000314902.5:n.205+4033_205+4034del
ENST00000323274.14:c.280-166_280-165del	ENSP00000315644.10:n.280-166_280-165del
ENST00000579128.1:n.358-166_358-165del
NM_001071.2:c.280-166_280-165del , LRG_783t1:c.280-166_280-165del	NP_001062.1:n.280-166_280-165del
NM_001071.3:c.280-166_280-165del	NP_001062.1:n.280-166_280-165del
NM_001354867.1:c.280-166_280-165del	NP_001341796.1:n.280-166_280-165del
NM_001354868.1:c.205+4033_205+4034del	NP_001341797.1:n.205+4033_205+4034del
NM_001071.4:c.280-166_280-165del MANE Select	NP_001062.1:n.280-166_280-165del
NM_001354867.2:c.280-166_280-165del	NP_001341796.1:n.280-166_280-165del
NM_001354868.2:c.205+4033_205+4034del	NP_001341797.1:n.205+4033_205+4034del