Canonical Allele Identifier: CA419137739

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97700414G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97234858G>A , CM000663.2:g.97234858G>A	GRCh38
NC_000001.10:g.97700414G>A , CM000663.1:g.97700414G>A	GRCh37
NC_000001.9:g.97473002G>A	NCBI36
NG_008807.2:g.691202C>T , LRG_722:g.691202C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2436C>T (DPYD) MANE Select	ENSP00000359211.3:p.Val812=
ENST00000370192.7:c.2436C>T (DPYD)	ENSP00000359211.3:p.Val812=
NM_000110.3:c.2436C>T , LRG_722t1:c.2436C>T (DPYD)	NP_000101.2:p.Val812=
NR_046590.1:n.65-30556G>A (DPYD-AS1)
XM_005270562.3:c.2220C>T (DPYD)	XP_005270619.2:p.Val740=
XM_006710397.2:c.2436C>T (DPYD)	XP_006710460.1:p.Val812=
XM_006710397.3:c.2436C>T (DPYD)	XP_006710460.1:p.Val812=
XM_017000507.1:c.2325C>T (DPYD)	XP_016855996.1:p.Val775=
XM_017000508.2:c.1941C>T (DPYD)	XP_016855997.1:p.Val647=
XM_017000509.2:c.1941C>T (DPYD)	XP_016855998.1:p.Val647=
XM_017000510.1:c.1941C>T (DPYD)	XP_016855999.1:p.Val647=
NM_000110.4:c.2436C>T (DPYD) MANE Select	NP_000101.2:p.Val812=