Canonical Allele Identifier: CA2521510042

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691405_97691406insTA , CM000663.2:g.97691405_97691406insTA	GRCh38
NC_000001.10:g.98156961_98156962insTA , CM000663.1:g.98156961_98156962insTA	GRCh37
NC_000001.9:g.97929549_97929550insTA	NCBI36
NG_008807.2:g.234654_234655insTA , LRG_722:g.234654_234655insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+311_762+312insTA MANE Select	ENSP00000359211.3:n.762+311_762+312insTA
ENST00000370192.7:c.762+311_762+312insTA	ENSP00000359211.3:n.762+311_762+312insTA
ENST00000474241.1:n.837_838insTA
NM_000110.3:c.762+311_762+312insTA , LRG_722t1:c.762+311_762+312insTA	NP_000101.2:n.762+311_762+312insTA
XM_005270562.3:c.762+311_762+312insTA	XP_005270619.2:n.762+311_762+312insTA
XM_006710397.2:c.762+311_762+312insTA	XP_006710460.1:n.762+311_762+312insTA
XM_006710397.3:c.762+311_762+312insTA	XP_006710460.1:n.762+311_762+312insTA
XM_017000507.1:c.651+311_651+312insTA	XP_016855996.1:n.651+311_651+312insTA
XM_017000508.2:c.267+311_267+312insTA	XP_016855997.1:n.267+311_267+312insTA
XM_017000509.2:c.267+311_267+312insTA	XP_016855998.1:n.267+311_267+312insTA
XM_017000510.1:c.267+311_267+312insTA	XP_016855999.1:n.267+311_267+312insTA
NM_000110.4:c.762+311_762+312insTA MANE Select	NP_000101.2:n.762+311_762+312insTA