Canonical Allele Identifier: CA2565326240

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549754_97549755del , CM000663.2:g.97549754_97549755del	GRCh38
NC_000001.10:g.98015310_98015311del , CM000663.1:g.98015310_98015311del	GRCh37
NC_000001.9:g.97787898_97787899del	NCBI36
NG_008807.2:g.376306_376307del , LRG_722:g.376306_376307del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1340-10_1340-9del MANE Select	ENSP00000359211.3:n.1340-10_1340-9del
ENST00000370192.7:c.1340-10_1340-9del	ENSP00000359211.3:n.1340-10_1340-9del
NM_000110.3:c.1340-10_1340-9del , LRG_722t1:c.1340-10_1340-9del	NP_000101.2:n.1340-10_1340-9del
XM_005270562.3:c.1340-10_1340-9del	XP_005270619.2:n.1340-10_1340-9del
XM_006710397.2:c.1340-10_1340-9del	XP_006710460.1:n.1340-10_1340-9del
XM_006710397.3:c.1340-10_1340-9del	XP_006710460.1:n.1340-10_1340-9del
XM_017000507.1:c.1229-10_1229-9del	XP_016855996.1:n.1229-10_1229-9del
XM_017000508.2:c.845-10_845-9del	XP_016855997.1:n.845-10_845-9del
XM_017000509.2:c.845-10_845-9del	XP_016855998.1:n.845-10_845-9del
XM_017000510.1:c.845-10_845-9del	XP_016855999.1:n.845-10_845-9del
NM_000110.4:c.1340-10_1340-9del MANE Select	NP_000101.2:n.1340-10_1340-9del