Canonical Allele Identifier: CA2646705301

Gene: DPYD

Linked Data

• gnomAD v4: 1-97382588-AAAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382591_97382593del , CM000663.2:g.97382591_97382593del	GRCh38
NC_000001.10:g.97848147_97848149del , CM000663.1:g.97848147_97848149del	GRCh37
NC_000001.9:g.97620735_97620737del	NCBI36
NG_008807.2:g.543469_543471del , LRG_722:g.543469_543471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1906-130_1906-128del MANE Select	ENSP00000359211.3:n.1906-130_1906-128del
ENST00000370192.7:c.1906-130_1906-128del	ENSP00000359211.3:n.1906-130_1906-128del
NM_000110.3:c.1906-130_1906-128del , LRG_722t1:c.1906-130_1906-128del	NP_000101.2:n.1906-130_1906-128del
XM_005270562.3:c.1690-130_1690-128del	XP_005270619.2:n.1690-130_1690-128del
XM_006710397.2:c.1906-130_1906-128del	XP_006710460.1:n.1906-130_1906-128del
XR_947619.1:n.1347-1043_1347-1041del
XR_947620.1:n.1125-1043_1125-1041del
XR_947621.1:n.1347-1043_1347-1041del
XM_006710397.3:c.1906-130_1906-128del	XP_006710460.1:n.1906-130_1906-128del
XM_017000507.1:c.1795-130_1795-128del	XP_016855996.1:n.1795-130_1795-128del
XM_017000508.2:c.1411-130_1411-128del	XP_016855997.1:n.1411-130_1411-128del
XM_017000509.2:c.1411-130_1411-128del	XP_016855998.1:n.1411-130_1411-128del
XM_017000510.1:c.1411-130_1411-128del	XP_016855999.1:n.1411-130_1411-128del
XR_001737686.2:n.692-1043_692-1041del
XR_001737687.1:n.692-1043_692-1041del
XR_001737688.2:n.692-1043_692-1041del
NM_000110.4:c.1906-130_1906-128del MANE Select	NP_000101.2:n.1906-130_1906-128del