Canonical Allele Identifier: CA2646703419

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97098720-A-AAGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098720_97098721insAGGC , CM000663.2:g.97098720_97098721insAGGC	GRCh38
NC_000001.10:g.97564276_97564277insAGGC , CM000663.1:g.97564276_97564277insAGGC	GRCh37
NC_000001.9:g.97336864_97336865insAGGC	NCBI36
NG_008807.2:g.827339_827340insGCCT , LRG_722:g.827339_827340insGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2623-89_2623-88insGCCT (DPYD) MANE Select	ENSP00000359211.3:n.2623-89_2623-88insGCCT
ENST00000370192.7:c.2623-89_2623-88insGCCT (DPYD)	ENSP00000359211.3:n.2623-89_2623-88insGCCT
NM_000110.3:c.2623-89_2623-88insGCCT , LRG_722t1:c.2623-89_2623-88insGCCT (DPYD)	NP_000101.2:n.2623-89_2623-88insGCCT
NR_046590.1:n.64+2734_64+2735insAGGC (DPYD-AS1)
XM_005270562.3:c.2407-89_2407-88insGCCT (DPYD)	XP_005270619.2:n.2407-89_2407-88insGCCT
XM_017000507.1:c.2512-89_2512-88insGCCT (DPYD)	XP_016855996.1:n.2512-89_2512-88insGCCT
XM_017000508.2:c.2128-89_2128-88insGCCT (DPYD)	XP_016855997.1:n.2128-89_2128-88insGCCT
XM_017000509.2:c.2128-89_2128-88insGCCT (DPYD)	XP_016855998.1:n.2128-89_2128-88insGCCT
XM_017000510.1:c.2128-89_2128-88insGCCT (DPYD)	XP_016855999.1:n.2128-89_2128-88insGCCT
NM_000110.4:c.2623-89_2623-88insGCCT (DPYD) MANE Select	NP_000101.2:n.2623-89_2623-88insGCCT