Canonical Allele Identifier: CA963322

Gene: DPYD

Linked Data

• dbSNP Id: rs750122226
• ExAC: 1:98015069 CTTATCCA / C
• gnomAD v2: 1-98015069-CTTATCCA-C
• gnomAD v4: 1-97549513-CTTATCCA-C
• MyVariant Identifiers: chr1:g.98015070_98015076del (hg19) ; chr1:g.97549514_97549520del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549516_97549522del , CM000663.2:g.97549516_97549522del	GRCh38
NC_000001.10:g.98015072_98015078del , CM000663.1:g.98015072_98015078del	GRCh37
NC_000001.9:g.97787660_97787666del	NCBI36
NG_008807.2:g.376540_376546del , LRG_722:g.376540_376546del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1524+40_1524+46del MANE Select	ENSP00000359211.3:n.1524+40_1524+46del
ENST00000370192.7:c.1524+40_1524+46del	ENSP00000359211.3:n.1524+40_1524+46del
NM_000110.3:c.1524+40_1524+46del , LRG_722t1:c.1524+40_1524+46del	NP_000101.2:n.1524+40_1524+46del
XM_005270562.3:c.1524+40_1524+46del	XP_005270619.2:n.1524+40_1524+46del
XM_006710397.2:c.1524+40_1524+46del	XP_006710460.1:n.1524+40_1524+46del
XM_006710397.3:c.1524+40_1524+46del	XP_006710460.1:n.1524+40_1524+46del
XM_017000507.1:c.1413+40_1413+46del	XP_016855996.1:n.1413+40_1413+46del
XM_017000508.2:c.1029+40_1029+46del	XP_016855997.1:n.1029+40_1029+46del
XM_017000509.2:c.1029+40_1029+46del	XP_016855998.1:n.1029+40_1029+46del
XM_017000510.1:c.1029+40_1029+46del	XP_016855999.1:n.1029+40_1029+46del
NM_000110.4:c.1524+40_1524+46del MANE Select	NP_000101.2:n.1524+40_1524+46del