Canonical Allele Identifier: CA2523294679

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691821_97691822dup , CM000663.2:g.97691821_97691822dup	GRCh38
NC_000001.10:g.98157377_98157378dup , CM000663.1:g.98157377_98157378dup	GRCh37
NC_000001.9:g.97929965_97929966dup	NCBI36
NG_008807.2:g.234241_234242dup , LRG_722:g.234241_234242dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.681-21_681-20dup MANE Select	ENSP00000359211.3:n.681-21_681-20dup
ENST00000370192.7:c.681-21_681-20dup	ENSP00000359211.3:n.681-21_681-20dup
ENST00000474241.1:n.445-21_445-20dup
NM_000110.3:c.681-21_681-20dup , LRG_722t1:c.681-21_681-20dup	NP_000101.2:n.681-21_681-20dup
XM_005270562.3:c.681-21_681-20dup	XP_005270619.2:n.681-21_681-20dup
XM_006710397.2:c.681-21_681-20dup	XP_006710460.1:n.681-21_681-20dup
XM_006710397.3:c.681-21_681-20dup	XP_006710460.1:n.681-21_681-20dup
XM_017000507.1:c.570-21_570-20dup	XP_016855996.1:n.570-21_570-20dup
XM_017000508.2:c.186-21_186-20dup	XP_016855997.1:n.186-21_186-20dup
XM_017000509.2:c.186-21_186-20dup	XP_016855998.1:n.186-21_186-20dup
XM_017000510.1:c.186-21_186-20dup	XP_016855999.1:n.186-21_186-20dup
NM_000110.4:c.681-21_681-20dup MANE Select	NP_000101.2:n.681-21_681-20dup