Canonical Allele Identifier: CA419137740

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs775111222
• MyVariant Identifiers: chr1:g.97700417G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97234861G>C , CM000663.2:g.97234861G>C	GRCh38
NC_000001.10:g.97700417G>C , CM000663.1:g.97700417G>C	GRCh37
NC_000001.9:g.97473005G>C	NCBI36
NG_008807.2:g.691199C>G , LRG_722:g.691199C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2433C>G (DPYD) MANE Select	ENSP00000359211.3:p.Ser811=
ENST00000370192.7:c.2433C>G (DPYD)	ENSP00000359211.3:p.Ser811=
NM_000110.3:c.2433C>G , LRG_722t1:c.2433C>G (DPYD)	NP_000101.2:p.Ser811=
NR_046590.1:n.65-30553G>C (DPYD-AS1)
XM_005270562.3:c.2217C>G (DPYD)	XP_005270619.2:p.Ser739=
XM_006710397.2:c.2433C>G (DPYD)	XP_006710460.1:p.Ser811=
XM_006710397.3:c.2433C>G (DPYD)	XP_006710460.1:p.Ser811=
XM_017000507.1:c.2322C>G (DPYD)	XP_016855996.1:p.Ser774=
XM_017000508.2:c.1938C>G (DPYD)	XP_016855997.1:p.Ser646=
XM_017000509.2:c.1938C>G (DPYD)	XP_016855998.1:p.Ser646=
XM_017000510.1:c.1938C>G (DPYD)	XP_016855999.1:p.Ser646=
NM_000110.4:c.2433C>G (DPYD) MANE Select	NP_000101.2:p.Ser811=