Canonical Allele Identifier: CA1182843767

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382488_97382490delinsAAG , CM000663.2:g.97382488_97382490delinsAAG	GRCh38
NC_000001.10:g.97848044_97848046delinsAAG , CM000663.1:g.97848044_97848046delinsAAG	GRCh37
NC_000001.9:g.97620632_97620634delinsAAG	NCBI36
NG_008807.2:g.543570_543572delinsCTT , LRG_722:g.543570_543572delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1906-29_1906-27delinsCTT MANE Select	ENSP00000359211.3:n.1906-29_1906-27delinsCTT
ENST00000370192.7:c.1906-29_1906-27delinsCTT	ENSP00000359211.3:n.1906-29_1906-27delinsCTT
NM_000110.3:c.1906-29_1906-27delinsCTT , LRG_722t1:c.1906-29_1906-27delinsCTT	NP_000101.2:n.1906-29_1906-27delinsCTT
XM_005270562.3:c.1690-29_1690-27delinsCTT	XP_005270619.2:n.1690-29_1690-27delinsCTT
XM_006710397.2:c.1906-29_1906-27delinsCTT	XP_006710460.1:n.1906-29_1906-27delinsCTT
XR_947619.1:n.1347-1146_1347-1144delinsAAG
XR_947620.1:n.1125-1146_1125-1144delinsAAG
XR_947621.1:n.1347-1146_1347-1144delinsAAG
XM_006710397.3:c.1906-29_1906-27delinsCTT	XP_006710460.1:n.1906-29_1906-27delinsCTT
XM_017000507.1:c.1795-29_1795-27delinsCTT	XP_016855996.1:n.1795-29_1795-27delinsCTT
XM_017000508.2:c.1411-29_1411-27delinsCTT	XP_016855997.1:n.1411-29_1411-27delinsCTT
XM_017000509.2:c.1411-29_1411-27delinsCTT	XP_016855998.1:n.1411-29_1411-27delinsCTT
XM_017000510.1:c.1411-29_1411-27delinsCTT	XP_016855999.1:n.1411-29_1411-27delinsCTT
XR_001737686.2:n.692-1146_692-1144delinsAAG
XR_001737687.1:n.692-1146_692-1144delinsAAG
XR_001737688.2:n.692-1146_692-1144delinsAAG
NM_000110.4:c.1906-29_1906-27delinsCTT MANE Select	NP_000101.2:n.1906-29_1906-27delinsCTT