Canonical Allele Identifier: CA2540392558

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97573689_97573690insTC , CM000663.2:g.97573689_97573690insTC	GRCh38
NC_000001.10:g.98039245_98039246insTC , CM000663.1:g.98039245_98039246insTC	GRCh37
NC_000001.9:g.97811833_97811834insTC	NCBI36
NG_008807.2:g.352370_352371insGA , LRG_722:g.352370_352371insGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1339+70_1339+71insGA MANE Select	ENSP00000359211.3:n.1339+70_1339+71insGA
ENST00000370192.7:c.1339+70_1339+71insGA	ENSP00000359211.3:n.1339+70_1339+71insGA
NM_000110.3:c.1339+70_1339+71insGA , LRG_722t1:c.1339+70_1339+71insGA	NP_000101.2:n.1339+70_1339+71insGA
XM_005270562.3:c.1339+70_1339+71insGA	XP_005270619.2:n.1339+70_1339+71insGA
XM_006710397.2:c.1339+70_1339+71insGA	XP_006710460.1:n.1339+70_1339+71insGA
XM_006710397.3:c.1339+70_1339+71insGA	XP_006710460.1:n.1339+70_1339+71insGA
XM_017000507.1:c.1228+70_1228+71insGA	XP_016855996.1:n.1228+70_1228+71insGA
XM_017000508.2:c.844+70_844+71insGA	XP_016855997.1:n.844+70_844+71insGA
XM_017000509.2:c.844+70_844+71insGA	XP_016855998.1:n.844+70_844+71insGA
XM_017000510.1:c.844+70_844+71insGA	XP_016855999.1:n.844+70_844+71insGA
NM_000110.4:c.1339+70_1339+71insGA MANE Select	NP_000101.2:n.1339+70_1339+71insGA