Canonical Allele Identifier: CA913078543

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97658667_97658668del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193111_97193112del , CM000663.2:g.97193111_97193112del	GRCh38
NC_000001.10:g.97658667_97658668del , CM000663.1:g.97658667_97658668del	GRCh37
NC_000001.9:g.97431255_97431256del	NCBI36
NG_008807.2:g.732949_732950del , LRG_722:g.732949_732950del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2580_2581del (DPYD) MANE Select	ENSP00000359211.3:p.Lys861ArgfsTer9
ENST00000370192.7:c.2580_2581del (DPYD)	ENSP00000359211.3:p.Lys861ArgfsTer9
NM_000110.3:c.2580_2581del , LRG_722t1:c.2580_2581del (DPYD)	NP_000101.2:p.Lys861ArgfsTer9
NR_046590.1:n.65-72303_65-72302del (DPYD-AS1)
XM_005270562.3:c.2364_2365del (DPYD)	XP_005270619.2:p.Lys789ArgfsTer9
XM_006710397.2:c.2580_2581del (DPYD)	XP_006710460.1:p.Lys861ArgfsTer9
XM_006710397.3:c.2580_2581del (DPYD)	XP_006710460.1:p.Lys861ArgfsTer9
XM_017000507.1:c.2469_2470del (DPYD)	XP_016855996.1:p.Lys824ArgfsTer9
XM_017000508.2:c.2085_2086del (DPYD)	XP_016855997.1:p.Lys696ArgfsTer9
XM_017000509.2:c.2085_2086del (DPYD)	XP_016855998.1:p.Lys696ArgfsTer9
XM_017000510.1:c.2085_2086del (DPYD)	XP_016855999.1:p.Lys696ArgfsTer9
NM_000110.4:c.2580_2581del (DPYD) MANE Select	NP_000101.2:p.Lys861ArgfsTer9