Canonical Allele Identifier: CA2810715007

Gene: TYMS ENOSF1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.672717C>A , CM000680.2:g.672717C>A	GRCh38
NC_000018.9:g.672717C>A , CM000680.1:g.672717C>A	GRCh37
NC_000018.8:g.662717C>A	NCBI36
NG_028255.1:g.20114C>A , LRG_783:g.20114C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323274.15:c.805-143C>A (TYMS) MANE Select	ENSP00000315644.10:n.805-143C>A
ENST00000647584.2:c.*1588G>T (ENOSF1) MANE Select	ENSP00000497230.2:n.*1588G>T
ENST00000323224.7:c.703-143C>A (TYMS)	ENSP00000314727.7:n.703-143C>A
ENST00000323250.9:c.556-143C>A (TYMS)	ENSP00000314902.5:n.556-143C>A
ENST00000323274.14:c.805-143C>A (TYMS)	ENSP00000315644.10:n.805-143C>A
ENST00000383578.7:c.*504G>T (ENOSF1)	ENSP00000373072.3:n.*504G>T
ENST00000581920.1:n.383-143C>A (TYMS)
ENST00000584259.6:n.3947G>T (ENOSF1)
NM_001071.2:c.805-143C>A , LRG_783t1:c.805-143C>A (TYMS)	NP_001062.1:n.805-143C>A
NM_001126123.3:c.*504G>T (ENOSF1)	NP_001119595.1:n.*504G>T
NM_017512.5:c.*1588G>T (ENOSF1)	NP_059982.2:n.*1588G>T
NM_202758.3:c.*1588G>T (ENOSF1)	NP_974487.1:n.*1588G>T
XR_243810.3:n.1872G>T (ENOSF1)
XR_243811.2:n.1897G>T (ENOSF1)
XR_430041.2:n.1992G>T (ENOSF1)
NM_001071.3:c.805-143C>A (TYMS)	NP_001062.1:n.805-143C>A
NM_001354867.1:c.703-143C>A (TYMS)	NP_001341796.1:n.703-143C>A
NM_001354868.1:c.556-143C>A (TYMS)	NP_001341797.1:n.556-143C>A
NR_148706.1:n.1797G>T (ENOSF1)
NR_148707.1:n.1913G>T (ENOSF1)
NR_148708.1:n.2161G>T (ENOSF1)
NR_148709.1:n.1847G>T (ENOSF1)
NR_148710.1:n.1873G>T (ENOSF1)
NR_148711.1:n.1724G>T (ENOSF1)
NR_148712.1:n.2057G>T (ENOSF1)
XM_024451242.1:c.424-143C>A (TYMS)	XP_024307010.1:n.424-143C>A
XR_002958180.1:n.1625G>T (ENOSF1)
XR_430041.4:n.2011G>T (ENOSF1)
NM_001071.4:c.805-143C>A (TYMS) MANE Select	NP_001062.1:n.805-143C>A
NM_017512.7:c.*1588G>T (ENOSF1) MANE Select	NP_059982.2:n.*1588G>T
NM_001318760.2:c.*1588G>T (ENOSF1)	NP_001305689.1:n.*1588G>T
NM_001354065.2:c.*1588G>T (ENOSF1)	NP_001340994.1:n.*1588G>T
NM_001354066.2:c.*1588G>T (ENOSF1)	NP_001340995.1:n.*1588G>T
NM_001354067.2:c.*1588G>T (ENOSF1)	NP_001340996.1:n.*1588G>T
NM_001354068.2:c.*1588G>T (ENOSF1)	NP_001340997.1:n.*1588G>T
NM_001354867.2:c.703-143C>A (TYMS)	NP_001341796.1:n.703-143C>A
NM_001354868.2:c.556-143C>A (TYMS)	NP_001341797.1:n.556-143C>A
NM_202758.5:c.*1588G>T (ENOSF1)	NP_974487.2:n.*1588G>T
NR_148706.2:n.1763G>T (ENOSF1)
NR_148707.2:n.1879G>T (ENOSF1)
NR_148708.2:n.2127G>T (ENOSF1)
NR_148709.2:n.1813G>T (ENOSF1)
NR_148710.2:n.1839G>T (ENOSF1)
NR_148711.2:n.1690G>T (ENOSF1)
NR_148712.2:n.2023G>T (ENOSF1)