Canonical Allele Identifier: CA740830730

Gene: DPYD

Linked Data

• dbSNP Id: rs1165252268
• gnomAD v3: 1-97691367-T-TA
• gnomAD v4: 1-97691367-T-TA
• MyVariant Identifiers: chr1:g.98156923_98156924insA (hg19) ; chr1:g.97691367_97691368insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691369dup , CM000663.2:g.97691369dup	GRCh38
NC_000001.10:g.98156925dup , CM000663.1:g.98156925dup	GRCh37
NC_000001.9:g.97929513dup	NCBI36
NG_008807.2:g.234692dup , LRG_722:g.234692dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+349dup MANE Select	ENSP00000359211.3:n.762+349dup
ENST00000370192.7:c.762+349dup	ENSP00000359211.3:n.762+349dup
ENST00000474241.1:n.875dup
NM_000110.3:c.762+349dup , LRG_722t1:c.762+349dup	NP_000101.2:n.762+349dup
XM_005270562.3:c.762+349dup	XP_005270619.2:n.762+349dup
XM_006710397.2:c.762+349dup	XP_006710460.1:n.762+349dup
XM_006710397.3:c.762+349dup	XP_006710460.1:n.762+349dup
XM_017000507.1:c.651+349dup	XP_016855996.1:n.651+349dup
XM_017000508.2:c.267+349dup	XP_016855997.1:n.267+349dup
XM_017000509.2:c.267+349dup	XP_016855998.1:n.267+349dup
XM_017000510.1:c.267+349dup	XP_016855999.1:n.267+349dup
NM_000110.4:c.762+349dup MANE Select	NP_000101.2:n.762+349dup