Canonical Allele Identifier: CA341379186

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.98157277A>G (hg19) ; chr1:g.97691721A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691721A>G , CM000663.2:g.97691721A>G	GRCh38
NC_000001.10:g.98157277A>G , CM000663.1:g.98157277A>G	GRCh37
NC_000001.9:g.97929865A>G	NCBI36
NG_008807.2:g.234339T>C , LRG_722:g.234339T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.758T>C MANE Select	ENSP00000359211.3:p.Val253Ala
ENST00000370192.7:c.758T>C	ENSP00000359211.3:p.Val253Ala
ENST00000474241.1:n.522T>C
NM_000110.3:c.758T>C , LRG_722t1:c.758T>C	NP_000101.2:p.Val253Ala
XM_005270562.3:c.758T>C	XP_005270619.2:p.Val253Ala
XM_006710397.2:c.758T>C	XP_006710460.1:p.Val253Ala
XM_006710397.3:c.758T>C	XP_006710460.1:p.Val253Ala
XM_017000507.1:c.647T>C	XP_016855996.1:p.Val216Ala
XM_017000508.2:c.263T>C	XP_016855997.1:p.Val88Ala
XM_017000509.2:c.263T>C	XP_016855998.1:p.Val88Ala
XM_017000510.1:c.263T>C	XP_016855999.1:p.Val88Ala
NM_000110.4:c.758T>C MANE Select	NP_000101.2:p.Val253Ala