Canonical Allele Identifier: CA295420314

Gene: TYMS

Linked Data

• dbSNP Id: rs796677254
• MyVariant Identifiers: chr18:g.662070_662071insC (hg19) ; chr18:g.662070_662071insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.662070_662071insC , CM000680.2:g.662070_662071insC	GRCh38
NC_000018.9:g.662070_662071insC , CM000680.1:g.662070_662071insC	GRCh37
NC_000018.8:g.652070_652071insC	NCBI36
NG_028255.1:g.9467_9468insC , LRG_783:g.9467_9468insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323274.15:c.280-76_280-75insC MANE Select	ENSP00000315644.10:n.280-76_280-75insC
ENST00000323224.7:c.280-76_280-75insC	ENSP00000314727.7:n.280-76_280-75insC
ENST00000323250.9:c.205+4123_205+4124insC	ENSP00000314902.5:n.205+4123_205+4124insC
ENST00000323274.14:c.280-76_280-75insC	ENSP00000315644.10:n.280-76_280-75insC
ENST00000579128.1:n.358-76_358-75insC
NM_001071.2:c.280-76_280-75insC , LRG_783t1:c.280-76_280-75insC	NP_001062.1:n.280-76_280-75insC
NM_001071.3:c.280-76_280-75insC	NP_001062.1:n.280-76_280-75insC
NM_001354867.1:c.280-76_280-75insC	NP_001341796.1:n.280-76_280-75insC
NM_001354868.1:c.205+4123_205+4124insC	NP_001341797.1:n.205+4123_205+4124insC
NM_001071.4:c.280-76_280-75insC MANE Select	NP_001062.1:n.280-76_280-75insC
NM_001354867.2:c.280-76_280-75insC	NP_001341796.1:n.280-76_280-75insC
NM_001354868.2:c.205+4123_205+4124insC	NP_001341797.1:n.205+4123_205+4124insC