Canonical Allele Identifier: CA1140587708

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098821_97098825delinsAAAAA , CM000663.2:g.97098821_97098825delinsAAAAA	GRCh38
NC_000001.10:g.97564377_97564381delinsAAAAA , CM000663.1:g.97564377_97564381delinsAAAAA	GRCh37
NC_000001.9:g.97336965_97336969delinsAAAAA	NCBI36
NG_008807.2:g.827235_827239delinsTTTTT , LRG_722:g.827235_827239delinsTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2623-193_2623-189delinsTTTTT (DPYD) MANE Select	ENSP00000359211.3:n.2623-193_2623-189delinsTTTTT
ENST00000370192.7:c.2623-193_2623-189delinsTTTTT (DPYD)	ENSP00000359211.3:n.2623-193_2623-189delinsTTTTT
NM_000110.3:c.2623-193_2623-189delinsTTTTT , LRG_722t1:c.2623-193_2623-189delinsTTTTT (DPYD)	NP_000101.2:n.2623-193_2623-189delinsTTTTT
NR_046590.1:n.64+2835_64+2839delinsAAAAA (DPYD-AS1)
XM_005270562.3:c.2407-193_2407-189delinsTTTTT (DPYD)	XP_005270619.2:n.2407-193_2407-189delinsTTTTT
XM_017000507.1:c.2512-193_2512-189delinsTTTTT (DPYD)	XP_016855996.1:n.2512-193_2512-189delinsTTTTT
XM_017000508.2:c.2128-193_2128-189delinsTTTTT (DPYD)	XP_016855997.1:n.2128-193_2128-189delinsTTTTT
XM_017000509.2:c.2128-193_2128-189delinsTTTTT (DPYD)	XP_016855998.1:n.2128-193_2128-189delinsTTTTT
XM_017000510.1:c.2128-193_2128-189delinsTTTTT (DPYD)	XP_016855999.1:n.2128-193_2128-189delinsTTTTT
NM_000110.4:c.2623-193_2623-189delinsTTTTT (DPYD) MANE Select	NP_000101.2:n.2623-193_2623-189delinsTTTTT