Canonical Allele Identifier: CA341379199

Gene: DPYD

Linked Data

• gnomAD v4: 1-97691728-G-A
• MyVariant Identifiers: chr1:g.98157284G>A (hg19) ; chr1:g.97691728G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691728G>A , CM000663.2:g.97691728G>A	GRCh38
NC_000001.10:g.98157284G>A , CM000663.1:g.98157284G>A	GRCh37
NC_000001.9:g.97929872G>A	NCBI36
NG_008807.2:g.234332C>T , LRG_722:g.234332C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.751C>T MANE Select	ENSP00000359211.3:p.Leu251Phe
ENST00000370192.7:c.751C>T	ENSP00000359211.3:p.Leu251Phe
ENST00000474241.1:n.515C>T
NM_000110.3:c.751C>T , LRG_722t1:c.751C>T	NP_000101.2:p.Leu251Phe
XM_005270562.3:c.751C>T	XP_005270619.2:p.Leu251Phe
XM_006710397.2:c.751C>T	XP_006710460.1:p.Leu251Phe
XM_006710397.3:c.751C>T	XP_006710460.1:p.Leu251Phe
XM_017000507.1:c.640C>T	XP_016855996.1:p.Leu214Phe
XM_017000508.2:c.256C>T	XP_016855997.1:p.Leu86Phe
XM_017000509.2:c.256C>T	XP_016855998.1:p.Leu86Phe
XM_017000510.1:c.256C>T	XP_016855999.1:p.Leu86Phe
NM_000110.4:c.751C>T MANE Select	NP_000101.2:p.Leu251Phe