Canonical Allele Identifier: CA1004785536

Gene: DPYD

Linked Data

• dbSNP Id: rs1651130779
• gnomAD v3: 1-97549202-T-TACC
• gnomAD v4: 1-97549202-T-TACC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549205_97549207dup , CM000663.2:g.97549205_97549207dup	GRCh38
NC_000001.10:g.98014761_98014763dup , CM000663.1:g.98014761_98014763dup	GRCh37
NC_000001.9:g.97787349_97787351dup	NCBI36
NG_008807.2:g.376855_376857dup , LRG_722:g.376855_376857dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1524+355_1524+357dup MANE Select	ENSP00000359211.3:n.1524+355_1524+357dup
ENST00000370192.7:c.1524+355_1524+357dup	ENSP00000359211.3:n.1524+355_1524+357dup
NM_000110.3:c.1524+355_1524+357dup , LRG_722t1:c.1524+355_1524+357dup	NP_000101.2:n.1524+355_1524+357dup
XM_005270562.3:c.1524+355_1524+357dup	XP_005270619.2:n.1524+355_1524+357dup
XM_006710397.2:c.1524+355_1524+357dup	XP_006710460.1:n.1524+355_1524+357dup
XM_006710397.3:c.1524+355_1524+357dup	XP_006710460.1:n.1524+355_1524+357dup
XM_017000507.1:c.1413+355_1413+357dup	XP_016855996.1:n.1413+355_1413+357dup
XM_017000508.2:c.1029+355_1029+357dup	XP_016855997.1:n.1029+355_1029+357dup
XM_017000509.2:c.1029+355_1029+357dup	XP_016855998.1:n.1029+355_1029+357dup
XM_017000510.1:c.1029+355_1029+357dup	XP_016855999.1:n.1029+355_1029+357dup
NM_000110.4:c.1524+355_1524+357dup MANE Select	NP_000101.2:n.1524+355_1524+357dup