Canonical Allele Identifier: CA1182776942

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97234954_97234956delinsGGA , CM000663.2:g.97234954_97234956delinsGGA	GRCh38
NC_000001.10:g.97700510_97700512delinsGGA , CM000663.1:g.97700510_97700512delinsGGA	GRCh37
NC_000001.9:g.97473098_97473100delinsGGA	NCBI36
NG_008807.2:g.691104_691106delinsTCC , LRG_722:g.691104_691106delinsTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2338_2340delinsTCC (DPYD) MANE Select	ENSP00000359211.3:p.Ser780=
ENST00000370192.7:c.2338_2340delinsTCC (DPYD)	ENSP00000359211.3:p.Ser780=
NM_000110.3:c.2338_2340delinsTCC , LRG_722t1:c.2338_2340delinsTCC (DPYD)	NP_000101.2:p.Ser780=
NR_046590.1:n.65-30460_65-30458delinsGGA (DPYD-AS1)
XM_005270562.3:c.2122_2124delinsTCC (DPYD)	XP_005270619.2:p.Ser708=
XM_006710397.2:c.2338_2340delinsTCC (DPYD)	XP_006710460.1:p.Ser780=
XM_006710397.3:c.2338_2340delinsTCC (DPYD)	XP_006710460.1:p.Ser780=
XM_017000507.1:c.2227_2229delinsTCC (DPYD)	XP_016855996.1:p.Ser743=
XM_017000508.2:c.1843_1845delinsTCC (DPYD)	XP_016855997.1:p.Ser615=
XM_017000509.2:c.1843_1845delinsTCC (DPYD)	XP_016855998.1:p.Ser615=
XM_017000510.1:c.1843_1845delinsTCC (DPYD)	XP_016855999.1:p.Ser615=
NM_000110.4:c.2338_2340delinsTCC (DPYD) MANE Select	NP_000101.2:p.Ser780=