Canonical Allele Identifier: CA963360

Gene: DPYD

Linked Data

• dbSNP Id: rs751326196
• ExAC: 1:98015303 G / GA
• gnomAD v2: 1-98015303-G-GA
• gnomAD v4: 1-97549747-G-GA
• MyVariant Identifiers: chr1:g.98015303_98015304insA (hg19) ; chr1:g.97549747_97549748insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549753dup , CM000663.2:g.97549753dup	GRCh38
NC_000001.10:g.98015309dup , CM000663.1:g.98015309dup	GRCh37
NC_000001.9:g.97787897dup	NCBI36
NG_008807.2:g.376312dup , LRG_722:g.376312dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1340-4dup MANE Select	ENSP00000359211.3:n.1340-4dup
ENST00000370192.7:c.1340-4dup	ENSP00000359211.3:n.1340-4dup
NM_000110.3:c.1340-4dup , LRG_722t1:c.1340-4dup	NP_000101.2:n.1340-4dup
XM_005270562.3:c.1340-4dup	XP_005270619.2:n.1340-4dup
XM_006710397.2:c.1340-4dup	XP_006710460.1:n.1340-4dup
XM_006710397.3:c.1340-4dup	XP_006710460.1:n.1340-4dup
XM_017000507.1:c.1229-4dup	XP_016855996.1:n.1229-4dup
XM_017000508.2:c.845-4dup	XP_016855997.1:n.845-4dup
XM_017000509.2:c.845-4dup	XP_016855998.1:n.845-4dup
XM_017000510.1:c.845-4dup	XP_016855999.1:n.845-4dup
NM_000110.4:c.1340-4dup MANE Select	NP_000101.2:n.1340-4dup