Canonical Allele Identifier: CA2646703730

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97193345-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193347del , CM000663.2:g.97193347del	GRCh38
NC_000001.10:g.97658903del , CM000663.1:g.97658903del	GRCh37
NC_000001.9:g.97431491del	NCBI36
NG_008807.2:g.732714del , LRG_722:g.732714del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2443-98del (DPYD) MANE Select	ENSP00000359211.3:n.2443-98del
ENST00000370192.7:c.2443-98del (DPYD)	ENSP00000359211.3:n.2443-98del
NM_000110.3:c.2443-98del , LRG_722t1:c.2443-98del (DPYD)	NP_000101.2:n.2443-98del
NR_046590.1:n.65-72067del (DPYD-AS1)
XM_005270562.3:c.2227-98del (DPYD)	XP_005270619.2:n.2227-98del
XM_006710397.2:c.2443-98del (DPYD)	XP_006710460.1:n.2443-98del
XM_006710397.3:c.2443-98del (DPYD)	XP_006710460.1:n.2443-98del
XM_017000507.1:c.2332-98del (DPYD)	XP_016855996.1:n.2332-98del
XM_017000508.2:c.1948-98del (DPYD)	XP_016855997.1:n.1948-98del
XM_017000509.2:c.1948-98del (DPYD)	XP_016855998.1:n.1948-98del
XM_017000510.1:c.1948-98del (DPYD)	XP_016855999.1:n.1948-98del
NM_000110.4:c.2443-98del (DPYD) MANE Select	NP_000101.2:n.2443-98del