Canonical Allele Identifier: CA2646703690

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97193243-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193244dup , CM000663.2:g.97193244dup	GRCh38
NC_000001.10:g.97658800dup , CM000663.1:g.97658800dup	GRCh37
NC_000001.9:g.97431388dup	NCBI36
NG_008807.2:g.732816dup , LRG_722:g.732816dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2447dup (DPYD) MANE Select	ENSP00000359211.3:p.Cys816TrpfsTer29
ENST00000370192.7:c.2447dup (DPYD)	ENSP00000359211.3:p.Cys816TrpfsTer29
NM_000110.3:c.2447dup , LRG_722t1:c.2447dup (DPYD)	NP_000101.2:p.Cys816TrpfsTer29
NR_046590.1:n.65-72170dup (DPYD-AS1)
XM_005270562.3:c.2231dup (DPYD)	XP_005270619.2:p.Cys744TrpfsTer29
XM_006710397.2:c.2447dup (DPYD)	XP_006710460.1:p.Cys816TrpfsTer29
XM_006710397.3:c.2447dup (DPYD)	XP_006710460.1:p.Cys816TrpfsTer29
XM_017000507.1:c.2336dup (DPYD)	XP_016855996.1:p.Cys779TrpfsTer29
XM_017000508.2:c.1952dup (DPYD)	XP_016855997.1:p.Cys651TrpfsTer29
XM_017000509.2:c.1952dup (DPYD)	XP_016855998.1:p.Cys651TrpfsTer29
XM_017000510.1:c.1952dup (DPYD)	XP_016855999.1:p.Cys651TrpfsTer29
NM_000110.4:c.2447dup (DPYD) MANE Select	NP_000101.2:p.Cys816TrpfsTer29