Canonical Allele Identifier: CA341376035

Gene: DPYD

Linked Data

• dbSNP Id: rs2101792559
• MyVariant Identifiers: chr1:g.97915676T>A (hg19) ; chr1:g.97450120T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450120T>A , CM000663.2:g.97450120T>A	GRCh38
NC_000001.10:g.97915676T>A , CM000663.1:g.97915676T>A	GRCh37
NC_000001.9:g.97688264T>A	NCBI36
NG_008807.2:g.475940A>T , LRG_722:g.475940A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1844A>T MANE Select	ENSP00000359211.3:p.Glu615Val
ENST00000370192.7:c.1844A>T	ENSP00000359211.3:p.Glu615Val
NM_000110.3:c.1844A>T , LRG_722t1:c.1844A>T	NP_000101.2:p.Glu615Val
XM_005270562.3:c.1628A>T	XP_005270619.2:p.Glu543Val
XM_006710397.2:c.1844A>T	XP_006710460.1:p.Glu615Val
XM_006710397.3:c.1844A>T	XP_006710460.1:p.Glu615Val
XM_017000507.1:c.1733A>T	XP_016855996.1:p.Glu578Val
XM_017000508.2:c.1349A>T	XP_016855997.1:p.Glu450Val
XM_017000509.2:c.1349A>T	XP_016855998.1:p.Glu450Val
XM_017000510.1:c.1349A>T	XP_016855999.1:p.Glu450Val
NM_000110.4:c.1844A>T MANE Select	NP_000101.2:p.Glu615Val