Canonical Allele Identifier: CA27517661

Gene: DPYD

Linked Data

• dbSNP Id: rs939798348
• MyVariant Identifiers: chr1:g.98014796_98014797insT (hg19) ; chr1:g.97549240_97549241insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549246dup , CM000663.2:g.97549246dup	GRCh38
NC_000001.10:g.98014802dup , CM000663.1:g.98014802dup	GRCh37
NC_000001.9:g.97787390dup	NCBI36
NG_008807.2:g.376819dup , LRG_722:g.376819dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1524+319dup MANE Select	ENSP00000359211.3:n.1524+319dup
ENST00000370192.7:c.1524+319dup	ENSP00000359211.3:n.1524+319dup
NM_000110.3:c.1524+319dup , LRG_722t1:c.1524+319dup	NP_000101.2:n.1524+319dup
XM_005270562.3:c.1524+319dup	XP_005270619.2:n.1524+319dup
XM_006710397.2:c.1524+319dup	XP_006710460.1:n.1524+319dup
XM_006710397.3:c.1524+319dup	XP_006710460.1:n.1524+319dup
XM_017000507.1:c.1413+319dup	XP_016855996.1:n.1413+319dup
XM_017000508.2:c.1029+319dup	XP_016855997.1:n.1029+319dup
XM_017000509.2:c.1029+319dup	XP_016855998.1:n.1029+319dup
XM_017000510.1:c.1029+319dup	XP_016855999.1:n.1029+319dup
NM_000110.4:c.1524+319dup MANE Select	NP_000101.2:n.1524+319dup