Canonical Allele Identifier: CA1182717261

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098721_97098725delinsCAAAT , CM000663.2:g.97098721_97098725delinsCAAAT	GRCh38
NC_000001.10:g.97564277_97564281delinsCAAAT , CM000663.1:g.97564277_97564281delinsCAAAT	GRCh37
NC_000001.9:g.97336865_97336869delinsCAAAT	NCBI36
NG_008807.2:g.827335_827339delinsATTTG , LRG_722:g.827335_827339delinsATTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2623-93_2623-89delinsATTTG (DPYD) MANE Select	ENSP00000359211.3:n.2623-93_2623-89delinsATTTG
ENST00000370192.7:c.2623-93_2623-89delinsATTTG (DPYD)	ENSP00000359211.3:n.2623-93_2623-89delinsATTTG
NM_000110.3:c.2623-93_2623-89delinsATTTG , LRG_722t1:c.2623-93_2623-89delinsATTTG (DPYD)	NP_000101.2:n.2623-93_2623-89delinsATTTG
NR_046590.1:n.64+2735_64+2739delinsCAAAT (DPYD-AS1)
XM_005270562.3:c.2407-93_2407-89delinsATTTG (DPYD)	XP_005270619.2:n.2407-93_2407-89delinsATTTG
XM_017000507.1:c.2512-93_2512-89delinsATTTG (DPYD)	XP_016855996.1:n.2512-93_2512-89delinsATTTG
XM_017000508.2:c.2128-93_2128-89delinsATTTG (DPYD)	XP_016855997.1:n.2128-93_2128-89delinsATTTG
XM_017000509.2:c.2128-93_2128-89delinsATTTG (DPYD)	XP_016855998.1:n.2128-93_2128-89delinsATTTG
XM_017000510.1:c.2128-93_2128-89delinsATTTG (DPYD)	XP_016855999.1:n.2128-93_2128-89delinsATTTG
NM_000110.4:c.2623-93_2623-89delinsATTTG (DPYD) MANE Select	NP_000101.2:n.2623-93_2623-89delinsATTTG