Canonical Allele Identifier: CA740787179

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1469736371
• gnomAD v3: 1-97098792-C-CTT
• gnomAD v4: 1-97098792-C-CTT
• MyVariant Identifiers: chr1:g.97564348_97564349insTT (hg19) ; chr1:g.97098792_97098793insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098793_97098794dup , CM000663.2:g.97098793_97098794dup	GRCh38
NC_000001.10:g.97564349_97564350dup , CM000663.1:g.97564349_97564350dup	GRCh37
NC_000001.9:g.97336937_97336938dup	NCBI36
NG_008807.2:g.827266_827267dup , LRG_722:g.827266_827267dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2623-162_2623-161dup (DPYD) MANE Select	ENSP00000359211.3:n.2623-162_2623-161dup
ENST00000370192.7:c.2623-162_2623-161dup (DPYD)	ENSP00000359211.3:n.2623-162_2623-161dup
NM_000110.3:c.2623-162_2623-161dup , LRG_722t1:c.2623-162_2623-161dup (DPYD)	NP_000101.2:n.2623-162_2623-161dup
NR_046590.1:n.64+2807_64+2808dup (DPYD-AS1)
XM_005270562.3:c.2407-162_2407-161dup (DPYD)	XP_005270619.2:n.2407-162_2407-161dup
XM_017000507.1:c.2512-162_2512-161dup (DPYD)	XP_016855996.1:n.2512-162_2512-161dup
XM_017000508.2:c.2128-162_2128-161dup (DPYD)	XP_016855997.1:n.2128-162_2128-161dup
XM_017000509.2:c.2128-162_2128-161dup (DPYD)	XP_016855998.1:n.2128-162_2128-161dup
XM_017000510.1:c.2128-162_2128-161dup (DPYD)	XP_016855999.1:n.2128-162_2128-161dup
NM_000110.4:c.2623-162_2623-161dup (DPYD) MANE Select	NP_000101.2:n.2623-162_2623-161dup