Canonical Allele Identifier: CA2640776978

Gene: TYMS ENOSF1

Linked Data

• gnomAD v4: 18-672796-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.672797_672798del , CM000680.2:g.672797_672798del	GRCh38
NC_000018.9:g.672797_672798del , CM000680.1:g.672797_672798del	GRCh37
NC_000018.8:g.662797_662798del	NCBI36
NG_028255.1:g.20194_20195del , LRG_783:g.20194_20195del

Transcript Alleles

HGVS	Amino-acid change
ENST00000323274.15:c.805-63_805-62del (TYMS) MANE Select	ENSP00000315644.10:n.805-63_805-62del
ENST00000647584.2:c.*1507_*1508del (ENOSF1) MANE Select	ENSP00000497230.2:n.*1507_*1508del
ENST00000323224.7:c.703-63_703-62del (TYMS)	ENSP00000314727.7:n.703-63_703-62del
ENST00000323250.9:c.556-63_556-62del (TYMS)	ENSP00000314902.5:n.556-63_556-62del
ENST00000323274.14:c.805-63_805-62del (TYMS)	ENSP00000315644.10:n.805-63_805-62del
ENST00000383578.7:c.*423_*424del (ENOSF1)	ENSP00000373072.3:n.*423_*424del
ENST00000581920.1:n.383-63_383-62del (TYMS)
ENST00000584259.6:n.3866_3867del (ENOSF1)
NM_001071.2:c.805-63_805-62del , LRG_783t1:c.805-63_805-62del (TYMS)	NP_001062.1:n.805-63_805-62del
NM_001126123.3:c.*423_*424del (ENOSF1)	NP_001119595.1:n.*423_*424del
NM_017512.5:c.*1507_*1508del (ENOSF1)	NP_059982.2:n.*1507_*1508del
NM_202758.3:c.*1507_*1508del (ENOSF1)	NP_974487.1:n.*1507_*1508del
XR_243810.3:n.1791_1792del (ENOSF1)
XR_243811.2:n.1816_1817del (ENOSF1)
XR_430041.2:n.1911_1912del (ENOSF1)
NM_001071.3:c.805-63_805-62del (TYMS)	NP_001062.1:n.805-63_805-62del
NM_001354867.1:c.703-63_703-62del (TYMS)	NP_001341796.1:n.703-63_703-62del
NM_001354868.1:c.556-63_556-62del (TYMS)	NP_001341797.1:n.556-63_556-62del
NR_148706.1:n.1716_1717del (ENOSF1)
NR_148707.1:n.1832_1833del (ENOSF1)
NR_148708.1:n.2080_2081del (ENOSF1)
NR_148709.1:n.1766_1767del (ENOSF1)
NR_148710.1:n.1792_1793del (ENOSF1)
NR_148711.1:n.1643_1644del (ENOSF1)
NR_148712.1:n.1976_1977del (ENOSF1)
XM_024451242.1:c.424-63_424-62del (TYMS)	XP_024307010.1:n.424-63_424-62del
XR_002958180.1:n.1544_1545del (ENOSF1)
XR_430041.4:n.1930_1931del (ENOSF1)
NM_001071.4:c.805-63_805-62del (TYMS) MANE Select	NP_001062.1:n.805-63_805-62del
NM_017512.7:c.*1507_*1508del (ENOSF1) MANE Select	NP_059982.2:n.*1507_*1508del
NM_001318760.2:c.*1507_*1508del (ENOSF1)	NP_001305689.1:n.*1507_*1508del
NM_001354065.2:c.*1507_*1508del (ENOSF1)	NP_001340994.1:n.*1507_*1508del
NM_001354066.2:c.*1507_*1508del (ENOSF1)	NP_001340995.1:n.*1507_*1508del
NM_001354067.2:c.*1507_*1508del (ENOSF1)	NP_001340996.1:n.*1507_*1508del
NM_001354068.2:c.*1507_*1508del (ENOSF1)	NP_001340997.1:n.*1507_*1508del
NM_001354867.2:c.703-63_703-62del (TYMS)	NP_001341796.1:n.703-63_703-62del
NM_001354868.2:c.556-63_556-62del (TYMS)	NP_001341797.1:n.556-63_556-62del
NM_202758.5:c.*1507_*1508del (ENOSF1)	NP_974487.2:n.*1507_*1508del
NR_148706.2:n.1682_1683del (ENOSF1)
NR_148707.2:n.1798_1799del (ENOSF1)
NR_148708.2:n.2046_2047del (ENOSF1)
NR_148709.2:n.1732_1733del (ENOSF1)
NR_148710.2:n.1758_1759del (ENOSF1)
NR_148711.2:n.1609_1610del (ENOSF1)
NR_148712.2:n.1942_1943del (ENOSF1)