Canonical Allele Identifier: CA419148262

Gene: DPYD

Linked Data

• gnomAD v4: 1-97828128-G-A
• MyVariant Identifiers: chr1:g.98293684G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828128G>A , CM000663.2:g.97828128G>A	GRCh38
NC_000001.10:g.98293684G>A , CM000663.1:g.98293684G>A	GRCh37
NC_000001.9:g.98066272G>A	NCBI36
NG_008807.2:g.97932C>T , LRG_722:g.97932C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.219C>T MANE Select	ENSP00000359211.3:p.Leu73=
ENST00000306031.5:c.219C>T	ENSP00000307107.5:p.Leu73=
ENST00000370192.7:c.219C>T	ENSP00000359211.3:p.Leu73=
NM_000110.3:c.219C>T , LRG_722t1:c.219C>T	NP_000101.2:p.Leu73=
NM_001160301.1:c.219C>T , LRG_722t2:c.219C>T	NP_001153773.1:p.Leu73=
XM_005270562.3:c.219C>T	XP_005270619.2:p.Leu73=
XM_006710397.2:c.219C>T	XP_006710460.1:p.Leu73=
XM_006710397.3:c.219C>T	XP_006710460.1:p.Leu73=
XM_017000507.1:c.108C>T	XP_016855996.1:p.Leu36=
XM_017000508.2:c.-492C>T	XP_016855997.1:n.-492C>T
XM_017000509.2:c.-390C>T	XP_016855998.1:n.-390C>T
XM_017000510.1:c.-390C>T	XP_016855999.1:n.-390C>T
XR_001737014.1:n.356C>T
NM_000110.4:c.219C>T MANE Select	NP_000101.2:p.Leu73=