Canonical Allele Identifier: CA1182717268

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1650447789

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098730G>A , CM000663.2:g.97098730G>A	GRCh38
NC_000001.10:g.97564286G>A , CM000663.1:g.97564286G>A	GRCh37
NC_000001.9:g.97336874G>A	NCBI36
NG_008807.2:g.827330C>T , LRG_722:g.827330C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2623-98C>T (DPYD) MANE Select	ENSP00000359211.3:n.2623-98C>T
ENST00000370192.7:c.2623-98C>T (DPYD)	ENSP00000359211.3:n.2623-98C>T
NM_000110.3:c.2623-98C>T , LRG_722t1:c.2623-98C>T (DPYD)	NP_000101.2:n.2623-98C>T
NR_046590.1:n.64+2744G>A (DPYD-AS1)
XM_005270562.3:c.2407-98C>T (DPYD)	XP_005270619.2:n.2407-98C>T
XM_017000507.1:c.2512-98C>T (DPYD)	XP_016855996.1:n.2512-98C>T
XM_017000508.2:c.2128-98C>T (DPYD)	XP_016855997.1:n.2128-98C>T
XM_017000509.2:c.2128-98C>T (DPYD)	XP_016855998.1:n.2128-98C>T
XM_017000510.1:c.2128-98C>T (DPYD)	XP_016855999.1:n.2128-98C>T
NM_000110.4:c.2623-98C>T (DPYD) MANE Select	NP_000101.2:n.2623-98C>T