Canonical Allele Identifier: CA419148263

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.98293684G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828128G>C , CM000663.2:g.97828128G>C	GRCh38
NC_000001.10:g.98293684G>C , CM000663.1:g.98293684G>C	GRCh37
NC_000001.9:g.98066272G>C	NCBI36
NG_008807.2:g.97932C>G , LRG_722:g.97932C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.219C>G MANE Select	ENSP00000359211.3:p.Leu73=
ENST00000306031.5:c.219C>G	ENSP00000307107.5:p.Leu73=
ENST00000370192.7:c.219C>G	ENSP00000359211.3:p.Leu73=
NM_000110.3:c.219C>G , LRG_722t1:c.219C>G	NP_000101.2:p.Leu73=
NM_001160301.1:c.219C>G , LRG_722t2:c.219C>G	NP_001153773.1:p.Leu73=
XM_005270562.3:c.219C>G	XP_005270619.2:p.Leu73=
XM_006710397.2:c.219C>G	XP_006710460.1:p.Leu73=
XM_006710397.3:c.219C>G	XP_006710460.1:p.Leu73=
XM_017000507.1:c.108C>G	XP_016855996.1:p.Leu36=
XM_017000508.2:c.-492C>G	XP_016855997.1:n.-492C>G
XM_017000509.2:c.-390C>G	XP_016855998.1:n.-390C>G
XM_017000510.1:c.-390C>G	XP_016855999.1:n.-390C>G
XR_001737014.1:n.356C>G
NM_000110.4:c.219C>G MANE Select	NP_000101.2:p.Leu73=