Canonical Allele Identifier: CA962978

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs745451696
• ExAC: 1:97564219 T / TGTTA
• gnomAD v2: 1-97564219-T-TGTTA
• gnomAD v3: 1-97098663-T-TGTTA
• gnomAD v4: 1-97098663-T-TGTTA
• MyVariant Identifiers: chr1:g.97564219_97564220insGTTA (hg19) ; chr1:g.97098663_97098664insGTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098665_97098668dup , CM000663.2:g.97098665_97098668dup	GRCh38
NC_000001.10:g.97564221_97564224dup , CM000663.1:g.97564221_97564224dup	GRCh37
NC_000001.9:g.97336809_97336812dup	NCBI36
NG_008807.2:g.827393_827396dup , LRG_722:g.827393_827396dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2623-35_2623-32dup (DPYD) MANE Select	ENSP00000359211.3:n.2623-35_2623-32dup
ENST00000370192.7:c.2623-35_2623-32dup (DPYD)	ENSP00000359211.3:n.2623-35_2623-32dup
NM_000110.3:c.2623-35_2623-32dup , LRG_722t1:c.2623-35_2623-32dup (DPYD)	NP_000101.2:n.2623-35_2623-32dup
NR_046590.1:n.64+2679_64+2682dup (DPYD-AS1)
XM_005270562.3:c.2407-35_2407-32dup (DPYD)	XP_005270619.2:n.2407-35_2407-32dup
XM_017000507.1:c.2512-35_2512-32dup (DPYD)	XP_016855996.1:n.2512-35_2512-32dup
XM_017000508.2:c.2128-35_2128-32dup (DPYD)	XP_016855997.1:n.2128-35_2128-32dup
XM_017000509.2:c.2128-35_2128-32dup (DPYD)	XP_016855998.1:n.2128-35_2128-32dup
XM_017000510.1:c.2128-35_2128-32dup (DPYD)	XP_016855999.1:n.2128-35_2128-32dup
NM_000110.4:c.2623-35_2623-32dup (DPYD) MANE Select	NP_000101.2:n.2623-35_2623-32dup