Canonical Allele Identifier: CA2646703689

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97193094-GGAAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193095_97193098del , CM000663.2:g.97193095_97193098del	GRCh38
NC_000001.10:g.97658651_97658654del , CM000663.1:g.97658651_97658654del	GRCh37
NC_000001.9:g.97431239_97431242del	NCBI36
NG_008807.2:g.732962_732965del , LRG_722:g.732962_732965del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2593_2596del (DPYD) MANE Select	ENSP00000359211.3:p.Val865HisfsTer3
ENST00000370192.7:c.2593_2596del (DPYD)	ENSP00000359211.3:p.Val865HisfsTer3
NM_000110.3:c.2593_2596del , LRG_722t1:c.2593_2596del (DPYD)	NP_000101.2:p.Val865HisfsTer3
NR_046590.1:n.65-72319_65-72316del (DPYD-AS1)
XM_005270562.3:c.2377_2380del (DPYD)	XP_005270619.2:p.Val793HisfsTer3
XM_006710397.2:c.2593_2596del (DPYD)	XP_006710460.1:p.Val865HisfsTer3
XM_006710397.3:c.2593_2596del (DPYD)	XP_006710460.1:p.Val865HisfsTer3
XM_017000507.1:c.2482_2485del (DPYD)	XP_016855996.1:p.Val828HisfsTer3
XM_017000508.2:c.2098_2101del (DPYD)	XP_016855997.1:p.Val700HisfsTer3
XM_017000509.2:c.2098_2101del (DPYD)	XP_016855998.1:p.Val700HisfsTer3
XM_017000510.1:c.2098_2101del (DPYD)	XP_016855999.1:p.Val700HisfsTer3
NM_000110.4:c.2593_2596del (DPYD) MANE Select	NP_000101.2:p.Val865HisfsTer3