Canonical Allele Identifier: CA525177561

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1348484901
• gnomAD v2: 1-97658632-ATGAGTTCAGCTATACG-A
• gnomAD v3: 1-97193076-ATGAGTTCAGCTATACG-A
• gnomAD v4: 1-97193076-ATGAGTTCAGCTATACG-A
• MyVariant Identifiers: chr1:g.97658633_97658648del (hg19) ; chr1:g.97193077_97193092del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193079_97193094del , CM000663.2:g.97193079_97193094del	GRCh38
NC_000001.10:g.97658635_97658650del , CM000663.1:g.97658635_97658650del	GRCh37
NC_000001.9:g.97431223_97431238del	NCBI36
NG_008807.2:g.732968_732983del , LRG_722:g.732968_732983del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2599_2614del (DPYD) MANE Select	ENSP00000359211.3:p.Arg867TrpfsTer19
ENST00000370192.7:c.2599_2614del (DPYD)	ENSP00000359211.3:p.Arg867TrpfsTer19
NM_000110.3:c.2599_2614del , LRG_722t1:c.2599_2614del (DPYD)	NP_000101.2:p.Arg867TrpfsTer19
NR_046590.1:n.65-72335_65-72320del (DPYD-AS1)
XM_005270562.3:c.2383_2398del (DPYD)	XP_005270619.2:p.Arg795TrpfsTer19
XM_006710397.2:c.2599_2614del (DPYD)	XP_006710460.1:p.Arg867TrpfsTer11
XM_006710397.3:c.2599_2614del (DPYD)	XP_006710460.1:p.Arg867TrpfsTer11
XM_017000507.1:c.2488_2503del (DPYD)	XP_016855996.1:p.Arg830TrpfsTer19
XM_017000508.2:c.2104_2119del (DPYD)	XP_016855997.1:p.Arg702TrpfsTer19
XM_017000509.2:c.2104_2119del (DPYD)	XP_016855998.1:p.Arg702TrpfsTer19
XM_017000510.1:c.2104_2119del (DPYD)	XP_016855999.1:p.Arg702TrpfsTer19
NM_000110.4:c.2599_2614del (DPYD) MANE Select	NP_000101.2:p.Arg867TrpfsTer19