Canonical Allele Identifier: CA341376023

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97915670G>T (hg19) ; chr1:g.97450114G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450114G>T , CM000663.2:g.97450114G>T	GRCh38
NC_000001.10:g.97915670G>T , CM000663.1:g.97915670G>T	GRCh37
NC_000001.9:g.97688258G>T	NCBI36
NG_008807.2:g.475946C>A , LRG_722:g.475946C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1850C>A MANE Select	ENSP00000359211.3:p.Thr617Lys
ENST00000370192.7:c.1850C>A	ENSP00000359211.3:p.Thr617Lys
NM_000110.3:c.1850C>A , LRG_722t1:c.1850C>A	NP_000101.2:p.Thr617Lys
XM_005270562.3:c.1634C>A	XP_005270619.2:p.Thr545Lys
XM_006710397.2:c.1850C>A	XP_006710460.1:p.Thr617Lys
XM_006710397.3:c.1850C>A	XP_006710460.1:p.Thr617Lys
XM_017000507.1:c.1739C>A	XP_016855996.1:p.Thr580Lys
XM_017000508.2:c.1355C>A	XP_016855997.1:p.Thr452Lys
XM_017000509.2:c.1355C>A	XP_016855998.1:p.Thr452Lys
XM_017000510.1:c.1355C>A	XP_016855999.1:p.Thr452Lys
NM_000110.4:c.1850C>A MANE Select	NP_000101.2:p.Thr617Lys