Canonical Allele Identifier: CA2646706990

Gene: DPYD

Linked Data

• gnomAD v4: 1-97691560-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691563dup , CM000663.2:g.97691563dup	GRCh38
NC_000001.10:g.98157119dup , CM000663.1:g.98157119dup	GRCh37
NC_000001.9:g.97929707dup	NCBI36
NG_008807.2:g.234499dup , LRG_722:g.234499dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.762+156dup MANE Select	ENSP00000359211.3:n.762+156dup
ENST00000370192.7:c.762+156dup	ENSP00000359211.3:n.762+156dup
ENST00000474241.1:n.682dup
NM_000110.3:c.762+156dup , LRG_722t1:c.762+156dup	NP_000101.2:n.762+156dup
XM_005270562.3:c.762+156dup	XP_005270619.2:n.762+156dup
XM_006710397.2:c.762+156dup	XP_006710460.1:n.762+156dup
XM_006710397.3:c.762+156dup	XP_006710460.1:n.762+156dup
XM_017000507.1:c.651+156dup	XP_016855996.1:n.651+156dup
XM_017000508.2:c.267+156dup	XP_016855997.1:n.267+156dup
XM_017000509.2:c.267+156dup	XP_016855998.1:n.267+156dup
XM_017000510.1:c.267+156dup	XP_016855999.1:n.267+156dup
NM_000110.4:c.762+156dup MANE Select	NP_000101.2:n.762+156dup