Canonical Allele Identifier: CA2586966989

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97234866-CACCACTATGGAGAAACTGAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97234873_97234893del , CM000663.2:g.97234873_97234893del	GRCh38
NC_000001.10:g.97700429_97700449del , CM000663.1:g.97700429_97700449del	GRCh37
NC_000001.9:g.97473017_97473037del	NCBI36
NG_008807.2:g.691173_691193del , LRG_722:g.691173_691193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2407_2427del (DPYD) MANE Select	ENSP00000359211.3:p.Leu803_Gly809del
ENST00000370192.7:c.2407_2427del (DPYD)	ENSP00000359211.3:p.Leu803_Gly809del
NM_000110.3:c.2407_2427del , LRG_722t1:c.2407_2427del (DPYD)	NP_000101.2:p.Leu803_Gly809del
NR_046590.1:n.65-30541_65-30521del (DPYD-AS1)
XM_005270562.3:c.2191_2211del (DPYD)	XP_005270619.2:p.Leu731_Gly737del
XM_006710397.2:c.2407_2427del (DPYD)	XP_006710460.1:p.Leu803_Gly809del
XM_006710397.3:c.2407_2427del (DPYD)	XP_006710460.1:p.Leu803_Gly809del
XM_017000507.1:c.2296_2316del (DPYD)	XP_016855996.1:p.Leu766_Gly772del
XM_017000508.2:c.1912_1932del (DPYD)	XP_016855997.1:p.Leu638_Gly644del
XM_017000509.2:c.1912_1932del (DPYD)	XP_016855998.1:p.Leu638_Gly644del
XM_017000510.1:c.1912_1932del (DPYD)	XP_016855999.1:p.Leu638_Gly644del
NM_000110.4:c.2407_2427del (DPYD) MANE Select	NP_000101.2:p.Leu803_Gly809del