Canonical Allele Identifier: CA2640776514

Gene: TYMS ENOSF1

Linked Data

• gnomAD v4: 18-672279-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.672279T>A , CM000680.2:g.672279T>A	GRCh38
NC_000018.9:g.672279T>A , CM000680.1:g.672279T>A	GRCh37
NC_000018.8:g.662279T>A	NCBI36
NG_028255.1:g.19676T>A , LRG_783:g.19676T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000323274.15:c.805-581T>A (TYMS) MANE Select	ENSP00000315644.10:n.805-581T>A
ENST00000647584.2:c.*2026A>T (ENOSF1) MANE Select	ENSP00000497230.2:n.*2026A>T
ENST00000323224.7:c.703-581T>A (TYMS)	ENSP00000314727.7:n.703-581T>A
ENST00000323250.9:c.556-581T>A (TYMS)	ENSP00000314902.5:n.556-581T>A
ENST00000323274.14:c.805-581T>A (TYMS)	ENSP00000315644.10:n.805-581T>A
ENST00000383578.7:c.*942A>T (ENOSF1)	ENSP00000373072.3:n.*942A>T
ENST00000581920.1:n.383-581T>A (TYMS)
ENST00000584259.6:n.4385A>T (ENOSF1)
NM_001071.2:c.805-581T>A , LRG_783t1:c.805-581T>A (TYMS)	NP_001062.1:n.805-581T>A
NM_001126123.3:c.*942A>T (ENOSF1)	NP_001119595.1:n.*942A>T
NM_017512.5:c.*2026A>T (ENOSF1)	NP_059982.2:n.*2026A>T
NM_202758.3:c.*2026A>T (ENOSF1)	NP_974487.1:n.*2026A>T
NM_001071.3:c.805-581T>A (TYMS)	NP_001062.1:n.805-581T>A
NM_001354867.1:c.703-581T>A (TYMS)	NP_001341796.1:n.703-581T>A
NM_001354868.1:c.556-581T>A (TYMS)	NP_001341797.1:n.556-581T>A
NR_148706.1:n.2235A>T (ENOSF1)
NR_148707.1:n.2351A>T (ENOSF1)
NR_148708.1:n.2599A>T (ENOSF1)
NR_148709.1:n.2285A>T (ENOSF1)
NR_148710.1:n.2311A>T (ENOSF1)
NR_148711.1:n.2162A>T (ENOSF1)
NR_148712.1:n.2495A>T (ENOSF1)
XM_024451242.1:c.424-581T>A (TYMS)	XP_024307010.1:n.424-581T>A
XR_002958180.1:n.2063A>T (ENOSF1)
XR_430041.4:n.2449A>T (ENOSF1)
NM_001071.4:c.805-581T>A (TYMS) MANE Select	NP_001062.1:n.805-581T>A
NM_017512.7:c.*2026A>T (ENOSF1) MANE Select	NP_059982.2:n.*2026A>T
NM_001318760.2:c.*2026A>T (ENOSF1)	NP_001305689.1:n.*2026A>T
NM_001354065.2:c.*2026A>T (ENOSF1)	NP_001340994.1:n.*2026A>T
NM_001354066.2:c.*2026A>T (ENOSF1)	NP_001340995.1:n.*2026A>T
NM_001354067.2:c.*2026A>T (ENOSF1)	NP_001340996.1:n.*2026A>T
NM_001354068.2:c.*2026A>T (ENOSF1)	NP_001340997.1:n.*2026A>T
NM_001354867.2:c.703-581T>A (TYMS)	NP_001341796.1:n.703-581T>A
NM_001354868.2:c.556-581T>A (TYMS)	NP_001341797.1:n.556-581T>A
NM_202758.5:c.*2026A>T (ENOSF1)	NP_974487.2:n.*2026A>T
NR_148706.2:n.2201A>T (ENOSF1)
NR_148707.2:n.2317A>T (ENOSF1)
NR_148708.2:n.2565A>T (ENOSF1)
NR_148709.2:n.2251A>T (ENOSF1)
NR_148710.2:n.2277A>T (ENOSF1)
NR_148711.2:n.2128A>T (ENOSF1)
NR_148712.2:n.2461A>T (ENOSF1)