Canonical Allele Identifier: CA341374784
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.97564092G>A (hg19) chr1:g.97098536G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098536G>A , CM000663.2:g.97098536G>A GRCh38
NC_000001.10:g.97564092G>A , CM000663.1:g.97564092G>A GRCh37
NC_000001.9:g.97336680G>A NCBI36
NG_008807.2:g.827524C>T , LRG_722:g.827524C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2719C>T (DPYD) MANE Select ENSP00000359211.3:p.Leu907Phe
ENST00000370192.7:c.2719C>T (DPYD) ENSP00000359211.3:p.Leu907Phe
NM_000110.3:c.2719C>T , LRG_722t1:c.2719C>T (DPYD) NP_000101.2:p.Leu907Phe
NR_046590.1:n.64+2550G>A (DPYD-AS1)
XM_005270562.3:c.2503C>T (DPYD) XP_005270619.2:p.Leu835Phe
XM_017000507.1:c.2608C>T (DPYD) XP_016855996.1:p.Leu870Phe
XM_017000508.2:c.2224C>T (DPYD) XP_016855997.1:p.Leu742Phe
XM_017000509.2:c.2224C>T (DPYD) XP_016855998.1:p.Leu742Phe
XM_017000510.1:c.2224C>T (DPYD) XP_016855999.1:p.Leu742Phe
NM_000110.4:c.2719C>T (DPYD) MANE Select NP_000101.2:p.Leu907Phe
Search 100 bp 5'
Search 100 bp 3'