Canonical Allele Identifier: CA27624769

Gene: DPYD

Linked Data

• dbSNP Id: rs945269985
• MyVariant Identifiers: chr1:g.98157351A>G (hg19) ; chr1:g.97691795A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691795A>G , CM000663.2:g.97691795A>G	GRCh38
NC_000001.10:g.98157351A>G , CM000663.1:g.98157351A>G	GRCh37
NC_000001.9:g.97929939A>G	NCBI36
NG_008807.2:g.234265T>C , LRG_722:g.234265T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.684T>C MANE Select	ENSP00000359211.3:p.Thr228=
ENST00000370192.7:c.684T>C	ENSP00000359211.3:p.Thr228=
ENST00000474241.1:n.448T>C
NM_000110.3:c.684T>C , LRG_722t1:c.684T>C	NP_000101.2:p.Thr228=
XM_005270562.3:c.684T>C	XP_005270619.2:p.Thr228=
XM_006710397.2:c.684T>C	XP_006710460.1:p.Thr228=
XM_006710397.3:c.684T>C	XP_006710460.1:p.Thr228=
XM_017000507.1:c.573T>C	XP_016855996.1:p.Thr191=
XM_017000508.2:c.189T>C	XP_016855997.1:p.Thr63=
XM_017000509.2:c.189T>C	XP_016855998.1:p.Thr63=
XM_017000510.1:c.189T>C	XP_016855999.1:p.Thr63=
NM_000110.4:c.684T>C MANE Select	NP_000101.2:p.Thr228=