Canonical Allele Identifier: CA419137014

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97564156C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098600C>T , CM000663.2:g.97098600C>T	GRCh38
NC_000001.10:g.97564156C>T , CM000663.1:g.97564156C>T	GRCh37
NC_000001.9:g.97336744C>T	NCBI36
NG_008807.2:g.827460G>A , LRG_722:g.827460G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2655G>A (DPYD) MANE Select	ENSP00000359211.3:p.Gln885=
ENST00000370192.7:c.2655G>A (DPYD)	ENSP00000359211.3:p.Gln885=
NM_000110.3:c.2655G>A , LRG_722t1:c.2655G>A (DPYD)	NP_000101.2:p.Gln885=
NR_046590.1:n.64+2614C>T (DPYD-AS1)
XM_005270562.3:c.2439G>A (DPYD)	XP_005270619.2:p.Gln813=
XM_017000507.1:c.2544G>A (DPYD)	XP_016855996.1:p.Gln848=
XM_017000508.2:c.2160G>A (DPYD)	XP_016855997.1:p.Gln720=
XM_017000509.2:c.2160G>A (DPYD)	XP_016855998.1:p.Gln720=
XM_017000510.1:c.2160G>A (DPYD)	XP_016855999.1:p.Gln720=
NM_000110.4:c.2655G>A (DPYD) MANE Select	NP_000101.2:p.Gln885=