Canonical Allele Identifier: CA1182979141

Gene: DPYD

Linked Data

• dbSNP Id: rs1660997879

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691322_97691325del , CM000663.2:g.97691322_97691325del	GRCh38
NC_000001.10:g.98156878_98156881del , CM000663.1:g.98156878_98156881del	GRCh37
NC_000001.9:g.97929466_97929469del	NCBI36
NG_008807.2:g.234738_234741del , LRG_722:g.234738_234741del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+395_762+398del MANE Select	ENSP00000359211.3:n.762+395_762+398del
ENST00000370192.7:c.762+395_762+398del	ENSP00000359211.3:n.762+395_762+398del
ENST00000474241.1:n.921_924del
NM_000110.3:c.762+395_762+398del , LRG_722t1:c.762+395_762+398del	NP_000101.2:n.762+395_762+398del
XM_005270562.3:c.762+395_762+398del	XP_005270619.2:n.762+395_762+398del
XM_006710397.2:c.762+395_762+398del	XP_006710460.1:n.762+395_762+398del
XM_006710397.3:c.762+395_762+398del	XP_006710460.1:n.762+395_762+398del
XM_017000507.1:c.651+395_651+398del	XP_016855996.1:n.651+395_651+398del
XM_017000508.2:c.267+395_267+398del	XP_016855997.1:n.267+395_267+398del
XM_017000509.2:c.267+395_267+398del	XP_016855998.1:n.267+395_267+398del
XM_017000510.1:c.267+395_267+398del	XP_016855999.1:n.267+395_267+398del
NM_000110.4:c.762+395_762+398del MANE Select	NP_000101.2:n.762+395_762+398del