Canonical Allele Identifier: CA2574442133

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305265del , CM000663.2:g.97305265del	GRCh38
NC_000001.10:g.97770821del , CM000663.1:g.97770821del	GRCh37
NC_000001.9:g.97543409del	NCBI36
NG_008807.2:g.620795del , LRG_722:g.620795del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2293del (DPYD) MANE Select	ENSP00000359211.3:p.Val765CysfsTer11
ENST00000370192.7:c.2293del (DPYD)	ENSP00000359211.3:p.Val765CysfsTer11
NM_000110.3:c.2293del , LRG_722t1:c.2293del (DPYD)	NP_000101.2:p.Val765CysfsTer11
NR_046590.1:n.129-924del (DPYD-AS1)
XM_005270562.3:c.2077del (DPYD)	XP_005270619.2:p.Val693CysfsTer11
XM_006710397.2:c.2293del (DPYD)	XP_006710460.1:p.Val765CysfsTer11
XM_006710397.3:c.2293del (DPYD)	XP_006710460.1:p.Val765CysfsTer11
XM_017000507.1:c.2182del (DPYD)	XP_016855996.1:p.Val728CysfsTer11
XM_017000508.2:c.1798del (DPYD)	XP_016855997.1:p.Val600CysfsTer11
XM_017000509.2:c.1798del (DPYD)	XP_016855998.1:p.Val600CysfsTer11
XM_017000510.1:c.1798del (DPYD)	XP_016855999.1:p.Val600CysfsTer11
NM_000110.4:c.2293del (DPYD) MANE Select	NP_000101.2:p.Val765CysfsTer11