Canonical Allele Identifier: CA341375594

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97839145T>A (hg19) ; chr1:g.97373589T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97373589T>A , CM000663.2:g.97373589T>A	GRCh38
NC_000001.10:g.97839145T>A , CM000663.1:g.97839145T>A	GRCh37
NC_000001.9:g.97611733T>A	NCBI36
NG_008807.2:g.552471A>T , LRG_722:g.552471A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2030A>T MANE Select	ENSP00000359211.3:p.Glu677Val
ENST00000370192.7:c.2030A>T	ENSP00000359211.3:p.Glu677Val
NM_000110.3:c.2030A>T , LRG_722t1:c.2030A>T	NP_000101.2:p.Glu677Val
XM_005270562.3:c.1814A>T	XP_005270619.2:p.Glu605Val
XM_006710397.2:c.2030A>T	XP_006710460.1:p.Glu677Val
XR_947619.1:n.1125-1939T>A
XR_947620.1:n.1124+6388T>A
XR_947621.1:n.1125-1939T>A
XM_006710397.3:c.2030A>T	XP_006710460.1:p.Glu677Val
XM_017000507.1:c.1919A>T	XP_016855996.1:p.Glu640Val
XM_017000508.2:c.1535A>T	XP_016855997.1:p.Glu512Val
XM_017000509.2:c.1535A>T	XP_016855998.1:p.Glu512Val
XM_017000510.1:c.1535A>T	XP_016855999.1:p.Glu512Val
NM_000110.4:c.2030A>T MANE Select	NP_000101.2:p.Glu677Val