Canonical Allele Identifier: CA341374898

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97098586-A-G
• MyVariant Identifiers: chr1:g.97564142A>G (hg19) ; chr1:g.97098586A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098586A>G , CM000663.2:g.97098586A>G	GRCh38
NC_000001.10:g.97564142A>G , CM000663.1:g.97564142A>G	GRCh37
NC_000001.9:g.97336730A>G	NCBI36
NG_008807.2:g.827474T>C , LRG_722:g.827474T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2669T>C (DPYD) MANE Select	ENSP00000359211.3:p.Ile890Thr
ENST00000370192.7:c.2669T>C (DPYD)	ENSP00000359211.3:p.Ile890Thr
NM_000110.3:c.2669T>C , LRG_722t1:c.2669T>C (DPYD)	NP_000101.2:p.Ile890Thr
NR_046590.1:n.64+2600A>G (DPYD-AS1)
XM_005270562.3:c.2453T>C (DPYD)	XP_005270619.2:p.Ile818Thr
XM_017000507.1:c.2558T>C (DPYD)	XP_016855996.1:p.Ile853Thr
XM_017000508.2:c.2174T>C (DPYD)	XP_016855997.1:p.Ile725Thr
XM_017000509.2:c.2174T>C (DPYD)	XP_016855998.1:p.Ile725Thr
XM_017000510.1:c.2174T>C (DPYD)	XP_016855999.1:p.Ile725Thr
NM_000110.4:c.2669T>C (DPYD) MANE Select	NP_000101.2:p.Ile890Thr