Canonical Allele Identifier: CA2744691400

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098620_97098621insCACACCCAACAC , CM000663.2:g.97098620_97098621insCACACCCAACAC	GRCh38
NC_000001.10:g.97564176_97564177insCACACCCAACAC , CM000663.1:g.97564176_97564177insCACACCCAACAC	GRCh37
NC_000001.9:g.97336764_97336765insCACACCCAACAC	NCBI36
NG_008807.2:g.827439_827440insGTGTTGGGTGTG , LRG_722:g.827439_827440insGTGTTGGGTGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2634_2635insGTGTTGGGTGTG (DPYD) MANE Select	ENSP00000359211.3:p.Ser878_Phe879insValLeuGlyVal
ENST00000370192.7:c.2634_2635insGTGTTGGGTGTG (DPYD)	ENSP00000359211.3:p.Ser878_Phe879insValLeuGlyVal
NM_000110.3:c.2634_2635insGTGTTGGGTGTG , LRG_722t1:c.2634_2635insGTGTTGGGTGTG (DPYD)	NP_000101.2:p.Ser878_Phe879insValLeuGlyVal
NR_046590.1:n.64+2634_64+2635insCACACCCAACAC (DPYD-AS1)
XM_005270562.3:c.2418_2419insGTGTTGGGTGTG (DPYD)	XP_005270619.2:p.Ser806_Phe807insValLeuGlyVal
XM_017000507.1:c.2523_2524insGTGTTGGGTGTG (DPYD)	XP_016855996.1:p.Ser841_Phe842insValLeuGlyVal
XM_017000508.2:c.2139_2140insGTGTTGGGTGTG (DPYD)	XP_016855997.1:p.Ser713_Phe714insValLeuGlyVal
XM_017000509.2:c.2139_2140insGTGTTGGGTGTG (DPYD)	XP_016855998.1:p.Ser713_Phe714insValLeuGlyVal
XM_017000510.1:c.2139_2140insGTGTTGGGTGTG (DPYD)	XP_016855999.1:p.Ser713_Phe714insValLeuGlyVal
NM_000110.4:c.2634_2635insGTGTTGGGTGTG (DPYD) MANE Select	NP_000101.2:p.Ser878_Phe879insValLeuGlyVal