Canonical Allele Identifier: CA2279754620

Gene: TYMS

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.668465C= , CM000680.2:g.668465C=	GRCh38
NC_000018.9:g.668465C= , CM000680.1:g.668465C=	GRCh37
NC_000018.8:g.658465C=	NCBI36
NG_028255.1:g.15862C= , LRG_783:g.15862C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001071.4:c.455-607C= MANE Select	NP_001062.1:n.455-607C=
ENST00000323274.15:c.455-607C= MANE Select	ENSP00000315644.10:n.455-607C=
NM_001071.2:c.455-607C= , LRG_783t1:c.455-607C=	NP_001062.1:n.455-607C=
NM_001071.3:c.455-607C=	NP_001062.1:n.455-607C=
NM_001354867.1:c.455-2227C=	NP_001341796.1:n.455-2227C=
NM_001354867.2:c.455-2227C=	NP_001341796.1:n.455-2227C=
NM_001354868.1:c.206-607C=	NP_001341797.1:n.206-607C=
NM_001354868.2:c.206-607C=	NP_001341797.1:n.206-607C=
ENST00000323224.7:c.455-2227C=	ENSP00000314727.7:n.455-2227C=
ENST00000323250.9:c.206-607C=	ENSP00000314902.5:n.206-607C=
ENST00000323274.14:c.455-607C=	ENSP00000315644.10:n.455-607C=
ENST00000579128.1:n.533-607C=
ENST00000581920.1:n.33-607C=
XM_024451242.1:c.74-607C=	XP_024307010.1:n.74-607C=