Canonical Allele Identifier: CA1182843813

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382570_97382571delinsAG , CM000663.2:g.97382570_97382571delinsAG	GRCh38
NC_000001.10:g.97848126_97848127delinsAG , CM000663.1:g.97848126_97848127delinsAG	GRCh37
NC_000001.9:g.97620714_97620715delinsAG	NCBI36
NG_008807.2:g.543489_543490delinsCT , LRG_722:g.543489_543490delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1906-110_1906-109delinsCT MANE Select	ENSP00000359211.3:n.1906-110_1906-109delinsCT
ENST00000370192.7:c.1906-110_1906-109delinsCT	ENSP00000359211.3:n.1906-110_1906-109delinsCT
NM_000110.3:c.1906-110_1906-109delinsCT , LRG_722t1:c.1906-110_1906-109delinsCT	NP_000101.2:n.1906-110_1906-109delinsCT
XM_005270562.3:c.1690-110_1690-109delinsCT	XP_005270619.2:n.1690-110_1690-109delinsCT
XM_006710397.2:c.1906-110_1906-109delinsCT	XP_006710460.1:n.1906-110_1906-109delinsCT
XR_947619.1:n.1347-1064_1347-1063delinsAG
XR_947620.1:n.1125-1064_1125-1063delinsAG
XR_947621.1:n.1347-1064_1347-1063delinsAG
XM_006710397.3:c.1906-110_1906-109delinsCT	XP_006710460.1:n.1906-110_1906-109delinsCT
XM_017000507.1:c.1795-110_1795-109delinsCT	XP_016855996.1:n.1795-110_1795-109delinsCT
XM_017000508.2:c.1411-110_1411-109delinsCT	XP_016855997.1:n.1411-110_1411-109delinsCT
XM_017000509.2:c.1411-110_1411-109delinsCT	XP_016855998.1:n.1411-110_1411-109delinsCT
XM_017000510.1:c.1411-110_1411-109delinsCT	XP_016855999.1:n.1411-110_1411-109delinsCT
XR_001737686.2:n.692-1064_692-1063delinsAG
XR_001737687.1:n.692-1064_692-1063delinsAG
XR_001737688.2:n.692-1064_692-1063delinsAG
NM_000110.4:c.1906-110_1906-109delinsCT MANE Select	NP_000101.2:n.1906-110_1906-109delinsCT