Canonical Allele Identifier: CA341374674

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97564043A>T (hg19) ; chr1:g.97098487A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098487A>T , CM000663.2:g.97098487A>T	GRCh38
NC_000001.10:g.97564043A>T , CM000663.1:g.97564043A>T	GRCh37
NC_000001.9:g.97336631A>T	NCBI36
NG_008807.2:g.827573T>A , LRG_722:g.827573T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2766+2T>A (DPYD) MANE Select	ENSP00000359211.3:n.2766+2T>A
ENST00000370192.7:c.2766+2T>A (DPYD)	ENSP00000359211.3:n.2766+2T>A
NM_000110.3:c.2766+2T>A , LRG_722t1:c.2766+2T>A (DPYD)	NP_000101.2:n.2766+2T>A
NR_046590.1:n.64+2501A>T (DPYD-AS1)
XM_005270562.3:c.2550+2T>A (DPYD)	XP_005270619.2:n.2550+2T>A
XM_017000507.1:c.2655+2T>A (DPYD)	XP_016855996.1:n.2655+2T>A
XM_017000508.2:c.2271+2T>A (DPYD)	XP_016855997.1:n.2271+2T>A
XM_017000509.2:c.2271+2T>A (DPYD)	XP_016855998.1:n.2271+2T>A
XM_017000510.1:c.2271+2T>A (DPYD)	XP_016855999.1:n.2271+2T>A
NM_000110.4:c.2766+2T>A (DPYD) MANE Select	NP_000101.2:n.2766+2T>A