Canonical Allele Identifier: CA2646706823

Gene: DPYD

Linked Data

• gnomAD v4: 1-97691281-GATT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691284_97691286del , CM000663.2:g.97691284_97691286del	GRCh38
NC_000001.10:g.98156840_98156842del , CM000663.1:g.98156840_98156842del	GRCh37
NC_000001.9:g.97929428_97929430del	NCBI36
NG_008807.2:g.234776_234778del , LRG_722:g.234776_234778del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+433_762+435del MANE Select	ENSP00000359211.3:n.762+433_762+435del
ENST00000370192.7:c.762+433_762+435del	ENSP00000359211.3:n.762+433_762+435del
ENST00000474241.1:n.959_961del
NM_000110.3:c.762+433_762+435del , LRG_722t1:c.762+433_762+435del	NP_000101.2:n.762+433_762+435del
XM_005270562.3:c.762+433_762+435del	XP_005270619.2:n.762+433_762+435del
XM_006710397.2:c.762+433_762+435del	XP_006710460.1:n.762+433_762+435del
XM_006710397.3:c.762+433_762+435del	XP_006710460.1:n.762+433_762+435del
XM_017000507.1:c.651+433_651+435del	XP_016855996.1:n.651+433_651+435del
XM_017000508.2:c.267+433_267+435del	XP_016855997.1:n.267+433_267+435del
XM_017000509.2:c.267+433_267+435del	XP_016855998.1:n.267+433_267+435del
XM_017000510.1:c.267+433_267+435del	XP_016855999.1:n.267+433_267+435del
NM_000110.4:c.762+433_762+435del MANE Select	NP_000101.2:n.762+433_762+435del