Canonical Allele Identifier: CA740786744

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1316126594
• gnomAD v3: 1-97098429-CT-C
• gnomAD v4: 1-97098429-CT-C
• MyVariant Identifiers: chr1:g.97563986del (hg19) ; chr1:g.97098430del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098430del , CM000663.2:g.97098430del	GRCh38
NC_000001.10:g.97563986del , CM000663.1:g.97563986del	GRCh37
NC_000001.9:g.97336574del	NCBI36
NG_008807.2:g.827630del , LRG_722:g.827630del

Transcript Alleles

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