Canonical Allele Identifier: CA2279747698

Gene: TYMS TYMSOS

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.657685G= , CM000680.2:g.657685G=	GRCh38
NC_000018.9:g.657685G= , CM000680.1:g.657685G=	GRCh37
NC_000018.8:g.647685G=	NCBI36
NG_028255.1:g.5082G= , LRG_783:g.5082G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001071.4:c.-58G= (TYMS) MANE Select	NP_001062.1:n.-58G=
ENST00000323274.15:c.-58G= (TYMS) MANE Select	ENSP00000315644.10:n.-58G=
NM_001012716.2:c.*34+157C= (TYMSOS)	NP_001012734.2:n.*34+157C=
NM_001012716.3:c.*34+157C= (TYMSOS)	NP_001012734.2:n.*34+157C=
NM_001071.2:c.-58G= , LRG_783t1:c.-58G= (TYMS)	NP_001062.1:n.-58G=
NM_001071.3:c.-58G= (TYMS)	NP_001062.1:n.-58G=
NM_001354867.1:c.-58G= (TYMS)	NP_001341796.1:n.-58G=
NM_001354867.2:c.-58G= (TYMS)	NP_001341796.1:n.-58G=
NM_001354868.1:c.-58G= (TYMS)	NP_001341797.1:n.-58G=
NM_001354868.2:c.-58G= (TYMS)	NP_001341797.1:n.-58G=
NR_171001.1:n.450+157C= (TYMSOS)
ENST00000323274.14:c.-58G= (TYMS)	ENSP00000315644.10:n.-58G=
ENST00000579128.1:n.21G= (TYMS)