Canonical Allele Identifier: CA1182979334

Gene: DPYD

Linked Data

• dbSNP Id: rs1661022602

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691822del , CM000663.2:g.97691822del	GRCh38
NC_000001.10:g.98157378del , CM000663.1:g.98157378del	GRCh37
NC_000001.9:g.97929966del	NCBI36
NG_008807.2:g.234242del , LRG_722:g.234242del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.681-20del MANE Select	ENSP00000359211.3:n.681-20del
ENST00000370192.7:c.681-20del	ENSP00000359211.3:n.681-20del
ENST00000474241.1:n.445-20del
NM_000110.3:c.681-20del , LRG_722t1:c.681-20del	NP_000101.2:n.681-20del
XM_005270562.3:c.681-20del	XP_005270619.2:n.681-20del
XM_006710397.2:c.681-20del	XP_006710460.1:n.681-20del
XM_006710397.3:c.681-20del	XP_006710460.1:n.681-20del
XM_017000507.1:c.570-20del	XP_016855996.1:n.570-20del
XM_017000508.2:c.186-20del	XP_016855997.1:n.186-20del
XM_017000509.2:c.186-20del	XP_016855998.1:n.186-20del
XM_017000510.1:c.186-20del	XP_016855999.1:n.186-20del
NM_000110.4:c.681-20del MANE Select	NP_000101.2:n.681-20del