Canonical Allele Identifier: CA1004765978

Gene: DPYD

Linked Data

• dbSNP Id: rs1020679489
• gnomAD v3: 1-97449907-C-CT
• gnomAD v4: 1-97449907-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97449913dup , CM000663.2:g.97449913dup	GRCh38
NC_000001.10:g.97915469dup , CM000663.1:g.97915469dup	GRCh37
NC_000001.9:g.97688057dup	NCBI36
NG_008807.2:g.476152dup , LRG_722:g.476152dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1905+151dup MANE Select	ENSP00000359211.3:n.1905+151dup
ENST00000370192.7:c.1905+151dup	ENSP00000359211.3:n.1905+151dup
NM_000110.3:c.1905+151dup , LRG_722t1:c.1905+151dup	NP_000101.2:n.1905+151dup
XM_005270562.3:c.1689+151dup	XP_005270619.2:n.1689+151dup
XM_006710397.2:c.1905+151dup	XP_006710460.1:n.1905+151dup
XM_006710397.3:c.1905+151dup	XP_006710460.1:n.1905+151dup
XM_017000507.1:c.1794+151dup	XP_016855996.1:n.1794+151dup
XM_017000508.2:c.1410+151dup	XP_016855997.1:n.1410+151dup
XM_017000509.2:c.1410+151dup	XP_016855998.1:n.1410+151dup
XM_017000510.1:c.1410+151dup	XP_016855999.1:n.1410+151dup
NM_000110.4:c.1905+151dup MANE Select	NP_000101.2:n.1905+151dup