Canonical Allele Identifier: CA2516748310

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97234928_97234929insCA , CM000663.2:g.97234928_97234929insCA	GRCh38
NC_000001.10:g.97700484_97700485insCA , CM000663.1:g.97700484_97700485insCA	GRCh37
NC_000001.9:g.97473072_97473073insCA	NCBI36
NG_008807.2:g.691131_691132insTG , LRG_722:g.691131_691132insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2365_2366insTG (DPYD) MANE Select	ENSP00000359211.3:p.Pro789LeufsTer?
ENST00000370192.7:c.2365_2366insTG (DPYD)	ENSP00000359211.3:p.Pro789LeufsTer?
NM_000110.3:c.2365_2366insTG , LRG_722t1:c.2365_2366insTG (DPYD)	NP_000101.2:p.Pro789LeufsTer?
NR_046590.1:n.65-30486_65-30485insCA (DPYD-AS1)
XM_005270562.3:c.2149_2150insTG (DPYD)	XP_005270619.2:p.Pro717LeufsTer?
XM_006710397.2:c.2365_2366insTG (DPYD)	XP_006710460.1:p.Pro789LeufsTer?
XM_006710397.3:c.2365_2366insTG (DPYD)	XP_006710460.1:p.Pro789LeufsTer?
XM_017000507.1:c.2254_2255insTG (DPYD)	XP_016855996.1:p.Pro752LeufsTer?
XM_017000508.2:c.1870_1871insTG (DPYD)	XP_016855997.1:p.Pro624LeufsTer?
XM_017000509.2:c.1870_1871insTG (DPYD)	XP_016855998.1:p.Pro624LeufsTer?
XM_017000510.1:c.1870_1871insTG (DPYD)	XP_016855999.1:p.Pro624LeufsTer?
NM_000110.4:c.2365_2366insTG (DPYD) MANE Select	NP_000101.2:p.Pro789LeufsTer?