Canonical Allele Identifier: CA1182717150

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098429_97098430delinsCT , CM000663.2:g.97098429_97098430delinsCT	GRCh38
NC_000001.10:g.97563985_97563986delinsCT , CM000663.1:g.97563985_97563986delinsCT	GRCh37
NC_000001.9:g.97336573_97336574delinsCT	NCBI36
NG_008807.2:g.827630_827631delinsAG , LRG_722:g.827630_827631delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2766+59_2766+60delinsAG (DPYD) MANE Select	ENSP00000359211.3:n.2766+59_2766+60delins...
ENST00000370192.7:c.2766+59_2766+60delinsAG (DPYD)	ENSP00000359211.3:n.2766+59_2766+60delins...
NM_000110.3:c.2766+59_2766+60delinsAG , LRG_722t1:c.2766+59_2766+60delinsAG (DPYD)	NP_000101.2:n.2766+59_2766+60delinsAG
NR_046590.1:n.64+2443_64+2444delinsCT (DPYD-AS1)
XM_005270562.3:c.2550+59_2550+60delinsAG (DPYD)	XP_005270619.2:n.2550+59_2550+60delinsAG
XM_017000507.1:c.2655+59_2655+60delinsAG (DPYD)	XP_016855996.1:n.2655+59_2655+60delinsAG
XM_017000508.2:c.2271+59_2271+60delinsAG (DPYD)	XP_016855997.1:n.2271+59_2271+60delinsAG
XM_017000509.2:c.2271+59_2271+60delinsAG (DPYD)	XP_016855998.1:n.2271+59_2271+60delinsAG
XM_017000510.1:c.2271+59_2271+60delinsAG (DPYD)	XP_016855999.1:n.2271+59_2271+60delinsAG
NM_000110.4:c.2766+59_2766+60delinsAG (DPYD) MANE Select	NP_000101.2:n.2766+59_2766+60delinsAG