Canonical Allele Identifier: CA1182843828

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382601_97382602delinsGA , CM000663.2:g.97382601_97382602delinsGA	GRCh38
NC_000001.10:g.97848157_97848158delinsGA , CM000663.1:g.97848157_97848158delinsGA	GRCh37
NC_000001.9:g.97620745_97620746delinsGA	NCBI36
NG_008807.2:g.543458_543459delinsTC , LRG_722:g.543458_543459delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1906-141_1906-140delinsTC MANE Select	ENSP00000359211.3:n.1906-141_1906-140delinsTC
ENST00000370192.7:c.1906-141_1906-140delinsTC	ENSP00000359211.3:n.1906-141_1906-140delinsTC
NM_000110.3:c.1906-141_1906-140delinsTC , LRG_722t1:c.1906-141_1906-140delinsTC	NP_000101.2:n.1906-141_1906-140delinsTC
XM_005270562.3:c.1690-141_1690-140delinsTC	XP_005270619.2:n.1690-141_1690-140delinsTC
XM_006710397.2:c.1906-141_1906-140delinsTC	XP_006710460.1:n.1906-141_1906-140delinsTC
XR_947619.1:n.1347-1033_1347-1032delinsGA
XR_947620.1:n.1125-1033_1125-1032delinsGA
XR_947621.1:n.1347-1033_1347-1032delinsGA
XM_006710397.3:c.1906-141_1906-140delinsTC	XP_006710460.1:n.1906-141_1906-140delinsTC
XM_017000507.1:c.1795-141_1795-140delinsTC	XP_016855996.1:n.1795-141_1795-140delinsTC
XM_017000508.2:c.1411-141_1411-140delinsTC	XP_016855997.1:n.1411-141_1411-140delinsTC
XM_017000509.2:c.1411-141_1411-140delinsTC	XP_016855998.1:n.1411-141_1411-140delinsTC
XM_017000510.1:c.1411-141_1411-140delinsTC	XP_016855999.1:n.1411-141_1411-140delinsTC
XR_001737686.2:n.692-1033_692-1032delinsGA
XR_001737687.1:n.692-1033_692-1032delinsGA
XR_001737688.2:n.692-1033_692-1032delinsGA
NM_000110.4:c.1906-141_1906-140delinsTC MANE Select	NP_000101.2:n.1906-141_1906-140delinsTC