Canonical Allele Identifier: CA2553712352

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382302_97382303insT , CM000663.2:g.97382302_97382303insT	GRCh38
NC_000001.10:g.97847858_97847859insT , CM000663.1:g.97847858_97847859insT	GRCh37
NC_000001.9:g.97620446_97620447insT	NCBI36
NG_008807.2:g.543757_543758insA , LRG_722:g.543757_543758insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1974+90_1974+91insA MANE Select	ENSP00000359211.3:n.1974+90_1974+91insA
ENST00000370192.7:c.1974+90_1974+91insA	ENSP00000359211.3:n.1974+90_1974+91insA
NM_000110.3:c.1974+90_1974+91insA , LRG_722t1:c.1974+90_1974+91insA	NP_000101.2:n.1974+90_1974+91insA
XM_005270562.3:c.1758+90_1758+91insA	XP_005270619.2:n.1758+90_1758+91insA
XM_006710397.2:c.1974+90_1974+91insA	XP_006710460.1:n.1974+90_1974+91insA
XR_947619.1:n.1347-1332_1347-1331insT
XR_947620.1:n.1125-1332_1125-1331insT
XR_947621.1:n.1347-1332_1347-1331insT
XM_006710397.3:c.1974+90_1974+91insA	XP_006710460.1:n.1974+90_1974+91insA
XM_017000507.1:c.1863+90_1863+91insA	XP_016855996.1:n.1863+90_1863+91insA
XM_017000508.2:c.1479+90_1479+91insA	XP_016855997.1:n.1479+90_1479+91insA
XM_017000509.2:c.1479+90_1479+91insA	XP_016855998.1:n.1479+90_1479+91insA
XM_017000510.1:c.1479+90_1479+91insA	XP_016855999.1:n.1479+90_1479+91insA
XR_001737686.2:n.692-1332_692-1331insT
XR_001737687.1:n.692-1332_692-1331insT
XR_001737688.2:n.692-1332_692-1331insT
NM_000110.4:c.1974+90_1974+91insA MANE Select	NP_000101.2:n.1974+90_1974+91insA