Canonical Allele Identifier: CA2574442392

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691696_97691699del , CM000663.2:g.97691696_97691699del	GRCh38
NC_000001.10:g.98157252_98157255del , CM000663.1:g.98157252_98157255del	GRCh37
NC_000001.9:g.97929840_97929843del	NCBI36
NG_008807.2:g.234363_234366del , LRG_722:g.234363_234366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+20_762+23del MANE Select	ENSP00000359211.3:n.762+20_762+23del
ENST00000370192.7:c.762+20_762+23del	ENSP00000359211.3:n.762+20_762+23del
ENST00000474241.1:n.546_549del
NM_000110.3:c.762+20_762+23del , LRG_722t1:c.762+20_762+23del	NP_000101.2:n.762+20_762+23del
XM_005270562.3:c.762+20_762+23del	XP_005270619.2:n.762+20_762+23del
XM_006710397.2:c.762+20_762+23del	XP_006710460.1:n.762+20_762+23del
XM_006710397.3:c.762+20_762+23del	XP_006710460.1:n.762+20_762+23del
XM_017000507.1:c.651+20_651+23del	XP_016855996.1:n.651+20_651+23del
XM_017000508.2:c.267+20_267+23del	XP_016855997.1:n.267+20_267+23del
XM_017000509.2:c.267+20_267+23del	XP_016855998.1:n.267+20_267+23del
XM_017000510.1:c.267+20_267+23del	XP_016855999.1:n.267+20_267+23del
NM_000110.4:c.762+20_762+23del MANE Select	NP_000101.2:n.762+20_762+23del