Canonical Allele Identifier: CA341377737

Gene: DPYD

Linked Data

• dbSNP Id: rs1206098971
• gnomAD v2: 1-98015214-C-T
• gnomAD v4: 1-97549658-C-T
• MyVariant Identifiers: chr1:g.98015214C>T (hg19) ; chr1:g.97549658C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549658C>T , CM000663.2:g.97549658C>T	GRCh38
NC_000001.10:g.98015214C>T , CM000663.1:g.98015214C>T	GRCh37
NC_000001.9:g.97787802C>T	NCBI36
NG_008807.2:g.376402G>A , LRG_722:g.376402G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1426G>A MANE Select	ENSP00000359211.3:p.Val476Ile
ENST00000370192.7:c.1426G>A	ENSP00000359211.3:p.Val476Ile
NM_000110.3:c.1426G>A , LRG_722t1:c.1426G>A	NP_000101.2:p.Val476Ile
XM_005270562.3:c.1426G>A	XP_005270619.2:p.Val476Ile
XM_006710397.2:c.1426G>A	XP_006710460.1:p.Val476Ile
XM_006710397.3:c.1426G>A	XP_006710460.1:p.Val476Ile
XM_017000507.1:c.1315G>A	XP_016855996.1:p.Val439Ile
XM_017000508.2:c.931G>A	XP_016855997.1:p.Val311Ile
XM_017000509.2:c.931G>A	XP_016855998.1:p.Val311Ile
XM_017000510.1:c.931G>A	XP_016855999.1:p.Val311Ile
NM_000110.4:c.1426G>A MANE Select	NP_000101.2:p.Val476Ile