Canonical Allele Identifier: CA341374976

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97098625-G-A
• MyVariant Identifiers: chr1:g.97564181G>A (hg19) ; chr1:g.97098625G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098625G>A , CM000663.2:g.97098625G>A	GRCh38
NC_000001.10:g.97564181G>A , CM000663.1:g.97564181G>A	GRCh37
NC_000001.9:g.97336769G>A	NCBI36
NG_008807.2:g.827435C>T , LRG_722:g.827435C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2630C>T (DPYD) MANE Select	ENSP00000359211.3:p.Pro877Leu
ENST00000370192.7:c.2630C>T (DPYD)	ENSP00000359211.3:p.Pro877Leu
NM_000110.3:c.2630C>T , LRG_722t1:c.2630C>T (DPYD)	NP_000101.2:p.Pro877Leu
NR_046590.1:n.64+2639G>A (DPYD-AS1)
XM_005270562.3:c.2414C>T (DPYD)	XP_005270619.2:p.Pro805Leu
XM_017000507.1:c.2519C>T (DPYD)	XP_016855996.1:p.Pro840Leu
XM_017000508.2:c.2135C>T (DPYD)	XP_016855997.1:p.Pro712Leu
XM_017000509.2:c.2135C>T (DPYD)	XP_016855998.1:p.Pro712Leu
XM_017000510.1:c.2135C>T (DPYD)	XP_016855999.1:p.Pro712Leu
NM_000110.4:c.2630C>T (DPYD) MANE Select	NP_000101.2:p.Pro877Leu