Canonical Allele Identifier: CA1182878215

Gene: DPYD

Linked Data

• dbSNP Id: rs1677023818

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97461373_97461374del , CM000663.2:g.97461373_97461374del	GRCh38
NC_000001.10:g.97926929_97926930del , CM000663.1:g.97926929_97926930del	GRCh37
NC_000001.9:g.97699517_97699518del	NCBI36
NG_008807.2:g.464687_464688del , LRG_722:g.464687_464688del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1741-11150_1741-11149del MANE Select	ENSP00000359211.3:n.1741-11150_1741-11149del
ENST00000370192.7:c.1741-11150_1741-11149del	ENSP00000359211.3:n.1741-11150_1741-11149del
NM_000110.3:c.1741-11150_1741-11149del , LRG_722t1:c.1741-11150_1741-11149del	NP_000101.2:n.1741-11150_1741-11149del
XM_005270562.3:c.1525-11150_1525-11149del	XP_005270619.2:n.1525-11150_1525-11149del
XM_006710397.2:c.1741-11150_1741-11149del	XP_006710460.1:n.1741-11150_1741-11149del
XM_006710397.3:c.1741-11150_1741-11149del	XP_006710460.1:n.1741-11150_1741-11149del
XM_017000507.1:c.1630-11150_1630-11149del	XP_016855996.1:n.1630-11150_1630-11149del
XM_017000508.2:c.1246-11150_1246-11149del	XP_016855997.1:n.1246-11150_1246-11149del
XM_017000509.2:c.1246-11150_1246-11149del	XP_016855998.1:n.1246-11150_1246-11149del
XM_017000510.1:c.1246-11150_1246-11149del	XP_016855999.1:n.1246-11150_1246-11149del
NM_000110.4:c.1741-11150_1741-11149del MANE Select	NP_000101.2:n.1741-11150_1741-11149del