Canonical Allele Identifier: CA2580607662

Gene: TYMS ENOSF1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.672363G>T , CM000680.2:g.672363G>T	GRCh38
NC_000018.9:g.672363G>T , CM000680.1:g.672363G>T	GRCh37
NC_000018.8:g.662363G>T	NCBI36
NG_028255.1:g.19760G>T , LRG_783:g.19760G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000323274.15:c.805-497G>T (TYMS) MANE Select	ENSP00000315644.10:n.805-497G>T
ENST00000647584.2:c.*1942C>A (ENOSF1) MANE Select	ENSP00000497230.2:n.*1942C>A
ENST00000323224.7:c.703-497G>T (TYMS)	ENSP00000314727.7:n.703-497G>T
ENST00000323250.9:c.556-497G>T (TYMS)	ENSP00000314902.5:n.556-497G>T
ENST00000323274.14:c.805-497G>T (TYMS)	ENSP00000315644.10:n.805-497G>T
ENST00000383578.7:c.*858C>A (ENOSF1)	ENSP00000373072.3:n.*858C>A
ENST00000581920.1:n.383-497G>T (TYMS)
ENST00000584259.6:n.4301C>A (ENOSF1)
NM_001071.2:c.805-497G>T , LRG_783t1:c.805-497G>T (TYMS)	NP_001062.1:n.805-497G>T
NM_001126123.3:c.*858C>A (ENOSF1)	NP_001119595.1:n.*858C>A
NM_017512.5:c.*1942C>A (ENOSF1)	NP_059982.2:n.*1942C>A
NM_202758.3:c.*1942C>A (ENOSF1)	NP_974487.1:n.*1942C>A
NM_001071.3:c.805-497G>T (TYMS)	NP_001062.1:n.805-497G>T
NM_001354867.1:c.703-497G>T (TYMS)	NP_001341796.1:n.703-497G>T
NM_001354868.1:c.556-497G>T (TYMS)	NP_001341797.1:n.556-497G>T
NR_148706.1:n.2151C>A (ENOSF1)
NR_148707.1:n.2267C>A (ENOSF1)
NR_148708.1:n.2515C>A (ENOSF1)
NR_148709.1:n.2201C>A (ENOSF1)
NR_148710.1:n.2227C>A (ENOSF1)
NR_148711.1:n.2078C>A (ENOSF1)
NR_148712.1:n.2411C>A (ENOSF1)
XM_024451242.1:c.424-497G>T (TYMS)	XP_024307010.1:n.424-497G>T
XR_002958180.1:n.1979C>A (ENOSF1)
XR_430041.4:n.2365C>A (ENOSF1)
NM_001071.4:c.805-497G>T (TYMS) MANE Select	NP_001062.1:n.805-497G>T
NM_017512.7:c.*1942C>A (ENOSF1) MANE Select	NP_059982.2:n.*1942C>A
NM_001318760.2:c.*1942C>A (ENOSF1)	NP_001305689.1:n.*1942C>A
NM_001354065.2:c.*1942C>A (ENOSF1)	NP_001340994.1:n.*1942C>A
NM_001354066.2:c.*1942C>A (ENOSF1)	NP_001340995.1:n.*1942C>A
NM_001354067.2:c.*1942C>A (ENOSF1)	NP_001340996.1:n.*1942C>A
NM_001354068.2:c.*1942C>A (ENOSF1)	NP_001340997.1:n.*1942C>A
NM_001354867.2:c.703-497G>T (TYMS)	NP_001341796.1:n.703-497G>T
NM_001354868.2:c.556-497G>T (TYMS)	NP_001341797.1:n.556-497G>T
NM_202758.5:c.*1942C>A (ENOSF1)	NP_974487.2:n.*1942C>A
NR_148706.2:n.2117C>A (ENOSF1)
NR_148707.2:n.2233C>A (ENOSF1)
NR_148708.2:n.2481C>A (ENOSF1)
NR_148709.2:n.2167C>A (ENOSF1)
NR_148710.2:n.2193C>A (ENOSF1)
NR_148711.2:n.2044C>A (ENOSF1)
NR_148712.2:n.2377C>A (ENOSF1)