Canonical Allele Identifier: CA419142481

Gene: DPYD

Linked Data

• dbSNP Id: rs751848058
• MyVariant Identifiers: chr1:g.97981336T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97515780T>C , CM000663.2:g.97515780T>C	GRCh38
NC_000001.10:g.97981336T>C , CM000663.1:g.97981336T>C	GRCh37
NC_000001.9:g.97753924T>C	NCBI36
NG_008807.2:g.410280A>G , LRG_722:g.410280A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1686A>G MANE Select	ENSP00000359211.3:p.Arg562=
ENST00000370192.7:c.1686A>G	ENSP00000359211.3:p.Arg562=
NM_000110.3:c.1686A>G , LRG_722t1:c.1686A>G	NP_000101.2:p.Arg562=
XM_005270562.3:c.1524+33780A>G	XP_005270619.2:n.1524+33780A>G
XM_006710397.2:c.1686A>G	XP_006710460.1:p.Arg562=
XM_006710397.3:c.1686A>G	XP_006710460.1:p.Arg562=
XM_017000507.1:c.1575A>G	XP_016855996.1:p.Arg525=
XM_017000508.2:c.1191A>G	XP_016855997.1:p.Arg397=
XM_017000509.2:c.1191A>G	XP_016855998.1:p.Arg397=
XM_017000510.1:c.1191A>G	XP_016855999.1:p.Arg397=
NM_000110.4:c.1686A>G MANE Select	NP_000101.2:p.Arg562=