Canonical Allele Identifier: CA341379400

Gene: DPYD

Linked Data

• gnomAD v4: 1-97828130-G-C
• MyVariant Identifiers: chr1:g.98293686G>C (hg19) ; chr1:g.97828130G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828130G>C , CM000663.2:g.97828130G>C	GRCh38
NC_000001.10:g.98293686G>C , CM000663.1:g.98293686G>C	GRCh37
NC_000001.9:g.98066274G>C	NCBI36
NG_008807.2:g.97930C>G , LRG_722:g.97930C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.217C>G MANE Select	ENSP00000359211.3:p.Leu73Val
ENST00000306031.5:c.217C>G	ENSP00000307107.5:p.Leu73Val
ENST00000370192.7:c.217C>G	ENSP00000359211.3:p.Leu73Val
NM_000110.3:c.217C>G , LRG_722t1:c.217C>G	NP_000101.2:p.Leu73Val
NM_001160301.1:c.217C>G , LRG_722t2:c.217C>G	NP_001153773.1:p.Leu73Val
XM_005270562.3:c.217C>G	XP_005270619.2:p.Leu73Val
XM_006710397.2:c.217C>G	XP_006710460.1:p.Leu73Val
XM_006710397.3:c.217C>G	XP_006710460.1:p.Leu73Val
XM_017000507.1:c.106C>G	XP_016855996.1:p.Leu36Val
XM_017000508.2:c.-494C>G	XP_016855997.1:n.-494C>G
XM_017000509.2:c.-392C>G	XP_016855998.1:n.-392C>G
XM_017000510.1:c.-392C>G	XP_016855999.1:n.-392C>G
XR_001737014.1:n.354C>G
NM_000110.4:c.217C>G MANE Select	NP_000101.2:p.Leu73Val