Canonical Allele Identifier: CA2279756872

Gene: TYMS ENOSF1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.672811C= , CM000680.2:g.672811C=	GRCh38
NC_000018.9:g.672811C= , CM000680.1:g.672811C=	GRCh37
NC_000018.8:g.662811C=	NCBI36
NG_028255.1:g.20208C= , LRG_783:g.20208C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000323274.15:c.805-49C= (TYMS) MANE Select	ENSP00000315644.10:n.805-49C=
ENST00000647584.2:c.*1494G= (ENOSF1) MANE Select	ENSP00000497230.2:n.*1494G=
ENST00000323224.7:c.703-49C= (TYMS)	ENSP00000314727.7:n.703-49C=
ENST00000323250.9:c.556-49C= (TYMS)	ENSP00000314902.5:n.556-49C=
ENST00000323274.14:c.805-49C= (TYMS)	ENSP00000315644.10:n.805-49C=
ENST00000383578.7:c.*410G= (ENOSF1)	ENSP00000373072.3:n.*410G=
ENST00000581920.1:n.383-49C= (TYMS)
ENST00000584259.6:n.3853G= (ENOSF1)
NM_001071.2:c.805-49C= , LRG_783t1:c.805-49C= (TYMS)	NP_001062.1:n.805-49C=
NM_001126123.3:c.*410G= (ENOSF1)	NP_001119595.1:n.*410G=
NM_017512.5:c.*1494G= (ENOSF1)	NP_059982.2:n.*1494G=
NM_202758.3:c.*1494G= (ENOSF1)	NP_974487.1:n.*1494G=
XR_243810.3:n.1778G= (ENOSF1)
XR_243811.2:n.1803G= (ENOSF1)
XR_430041.2:n.1898G= (ENOSF1)
NM_001071.3:c.805-49C= (TYMS)	NP_001062.1:n.805-49C=
NM_001354867.1:c.703-49C= (TYMS)	NP_001341796.1:n.703-49C=
NM_001354868.1:c.556-49C= (TYMS)	NP_001341797.1:n.556-49C=
NR_148706.1:n.1703G= (ENOSF1)
NR_148707.1:n.1819G= (ENOSF1)
NR_148708.1:n.2067G= (ENOSF1)
NR_148709.1:n.1753G= (ENOSF1)
NR_148710.1:n.1779G= (ENOSF1)
NR_148711.1:n.1630G= (ENOSF1)
NR_148712.1:n.1963G= (ENOSF1)
XM_024451242.1:c.424-49C= (TYMS)	XP_024307010.1:n.424-49C=
XR_002958180.1:n.1531G= (ENOSF1)
XR_430041.4:n.1917G= (ENOSF1)
NM_001071.4:c.805-49C= (TYMS) MANE Select	NP_001062.1:n.805-49C=
NM_017512.7:c.*1494G= (ENOSF1) MANE Select	NP_059982.2:n.*1494G=
NM_001318760.2:c.*1494G= (ENOSF1)	NP_001305689.1:n.*1494G=
NM_001354065.2:c.*1494G= (ENOSF1)	NP_001340994.1:n.*1494G=
NM_001354066.2:c.*1494G= (ENOSF1)	NP_001340995.1:n.*1494G=
NM_001354067.2:c.*1494G= (ENOSF1)	NP_001340996.1:n.*1494G=
NM_001354068.2:c.*1494G= (ENOSF1)	NP_001340997.1:n.*1494G=
NM_001354867.2:c.703-49C= (TYMS)	NP_001341796.1:n.703-49C=
NM_001354868.2:c.556-49C= (TYMS)	NP_001341797.1:n.556-49C=
NM_202758.5:c.*1494G= (ENOSF1)	NP_974487.2:n.*1494G=
NR_148706.2:n.1669G= (ENOSF1)
NR_148707.2:n.1785G= (ENOSF1)
NR_148708.2:n.2033G= (ENOSF1)
NR_148709.2:n.1719G= (ENOSF1)
NR_148710.2:n.1745G= (ENOSF1)
NR_148711.2:n.1596G= (ENOSF1)
NR_148712.2:n.1929G= (ENOSF1)