Canonical Allele Identifier: CA2646703366

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97098430-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098430T>G , CM000663.2:g.97098430T>G	GRCh38
NC_000001.10:g.97563986T>G , CM000663.1:g.97563986T>G	GRCh37
NC_000001.9:g.97336574T>G	NCBI36
NG_008807.2:g.827630A>C , LRG_722:g.827630A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2766+59A>C (DPYD) MANE Select	ENSP00000359211.3:n.2766+59A>C
ENST00000370192.7:c.2766+59A>C (DPYD)	ENSP00000359211.3:n.2766+59A>C
NM_000110.3:c.2766+59A>C , LRG_722t1:c.2766+59A>C (DPYD)	NP_000101.2:n.2766+59A>C
NR_046590.1:n.64+2444T>G (DPYD-AS1)
XM_005270562.3:c.2550+59A>C (DPYD)	XP_005270619.2:n.2550+59A>C
XM_017000507.1:c.2655+59A>C (DPYD)	XP_016855996.1:n.2655+59A>C
XM_017000508.2:c.2271+59A>C (DPYD)	XP_016855997.1:n.2271+59A>C
XM_017000509.2:c.2271+59A>C (DPYD)	XP_016855998.1:n.2271+59A>C
XM_017000510.1:c.2271+59A>C (DPYD)	XP_016855999.1:n.2271+59A>C
NM_000110.4:c.2766+59A>C (DPYD) MANE Select	NP_000101.2:n.2766+59A>C