Canonical Allele Identifier: CA2640777150

Gene: TYMS ENOSF1

Linked Data

• gnomAD v4: 18-673099-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.673103_673104del , CM000680.2:g.673103_673104del	GRCh38
NC_000018.9:g.673103_673104del , CM000680.1:g.673103_673104del	GRCh37
NC_000018.8:g.663103_663104del	NCBI36
NG_028255.1:g.20500_20501del , LRG_783:g.20500_20501del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323274.15:c.*106_*107del (TYMS) MANE Select	ENSP00000315644.10:n.*106_*107del
ENST00000647584.2:c.*1204_*1205del (ENOSF1) MANE Select	ENSP00000497230.2:n.*1204_*1205del
ENST00000323224.7:c.946_947del (TYMS)	ENSP00000314727.7:n.946_947del
ENST00000323274.14:c.*106_*107del (TYMS)	ENSP00000315644.10:n.*106_*107del
ENST00000383578.7:c.*145-25_*145-24del (ENOSF1)	ENSP00000373072.3:n.*145-25_*145-24del
ENST00000581920.1:n.626_627del (TYMS)
ENST00000584259.6:n.3588-25_3588-24del (ENOSF1)
NM_001071.2:c.*106_*107del , LRG_783t1:c.*106_*107del (TYMS)	NP_001062.1:n.*106_*107del
NM_001126123.3:c.*145-25_*145-24del (ENOSF1)	NP_001119595.1:n.*145-25_*145-24del
NM_017512.5:c.*1204_*1205del (ENOSF1)	NP_059982.2:n.*1204_*1205del
NM_202758.3:c.*1204_*1205del (ENOSF1)	NP_974487.1:n.*1204_*1205del
XR_243810.3:n.1513-25_1513-24del (ENOSF1)
XR_243811.2:n.1538-25_1538-24del (ENOSF1)
XR_430041.2:n.1633-25_1633-24del (ENOSF1)
NM_001071.3:c.*106_*107del (TYMS)	NP_001062.1:n.*106_*107del
NM_001354867.1:c.*106_*107del (TYMS)	NP_001341796.1:n.*106_*107del
NM_001354868.1:c.*106_*107del (TYMS)	NP_001341797.1:n.*106_*107del
NR_148706.1:n.1438-25_1438-24del (ENOSF1)
NR_148707.1:n.1554-25_1554-24del (ENOSF1)
NR_148708.1:n.1802-25_1802-24del (ENOSF1)
NR_148709.1:n.1488-25_1488-24del (ENOSF1)
NR_148710.1:n.1514-25_1514-24del (ENOSF1)
NR_148711.1:n.1365-25_1365-24del (ENOSF1)
NR_148712.1:n.1698-25_1698-24del (ENOSF1)
XM_024451242.1:c.*106_*107del (TYMS)	XP_024307010.1:n.*106_*107del
XR_002958180.1:n.1266-25_1266-24del (ENOSF1)
XR_430041.4:n.1652-25_1652-24del (ENOSF1)
NM_001071.4:c.*106_*107del (TYMS) MANE Select	NP_001062.1:n.*106_*107del
NM_017512.7:c.*1204_*1205del (ENOSF1) MANE Select	NP_059982.2:n.*1204_*1205del
NM_001318760.2:c.*1204_*1205del (ENOSF1)	NP_001305689.1:n.*1204_*1205del
NM_001354065.2:c.*1204_*1205del (ENOSF1)	NP_001340994.1:n.*1204_*1205del
NM_001354066.2:c.*1204_*1205del (ENOSF1)	NP_001340995.1:n.*1204_*1205del
NM_001354067.2:c.*1204_*1205del (ENOSF1)	NP_001340996.1:n.*1204_*1205del
NM_001354068.2:c.*1204_*1205del (ENOSF1)	NP_001340997.1:n.*1204_*1205del
NM_001354867.2:c.*106_*107del (TYMS)	NP_001341796.1:n.*106_*107del
NM_001354868.2:c.*106_*107del (TYMS)	NP_001341797.1:n.*106_*107del
NM_202758.5:c.*1204_*1205del (ENOSF1)	NP_974487.2:n.*1204_*1205del
NR_148706.2:n.1404-25_1404-24del (ENOSF1)
NR_148707.2:n.1520-25_1520-24del (ENOSF1)
NR_148708.2:n.1768-25_1768-24del (ENOSF1)
NR_148709.2:n.1454-25_1454-24del (ENOSF1)
NR_148710.2:n.1480-25_1480-24del (ENOSF1)
NR_148711.2:n.1331-25_1331-24del (ENOSF1)
NR_148712.2:n.1664-25_1664-24del (ENOSF1)