Canonical Allele Identifier: CA341379398

Gene: DPYD

Linked Data

• gnomAD v4: 1-97828129-A-G
• MyVariant Identifiers: chr1:g.98293685A>G (hg19) ; chr1:g.97828129A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828129A>G , CM000663.2:g.97828129A>G	GRCh38
NC_000001.10:g.98293685A>G , CM000663.1:g.98293685A>G	GRCh37
NC_000001.9:g.98066273A>G	NCBI36
NG_008807.2:g.97931T>C , LRG_722:g.97931T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.218T>C MANE Select	ENSP00000359211.3:p.Leu73Pro
ENST00000306031.5:c.218T>C	ENSP00000307107.5:p.Leu73Pro
ENST00000370192.7:c.218T>C	ENSP00000359211.3:p.Leu73Pro
NM_000110.3:c.218T>C , LRG_722t1:c.218T>C	NP_000101.2:p.Leu73Pro
NM_001160301.1:c.218T>C , LRG_722t2:c.218T>C	NP_001153773.1:p.Leu73Pro
XM_005270562.3:c.218T>C	XP_005270619.2:p.Leu73Pro
XM_006710397.2:c.218T>C	XP_006710460.1:p.Leu73Pro
XM_006710397.3:c.218T>C	XP_006710460.1:p.Leu73Pro
XM_017000507.1:c.107T>C	XP_016855996.1:p.Leu36Pro
XM_017000508.2:c.-493T>C	XP_016855997.1:n.-493T>C
XM_017000509.2:c.-391T>C	XP_016855998.1:n.-391T>C
XM_017000510.1:c.-391T>C	XP_016855999.1:n.-391T>C
XR_001737014.1:n.355T>C
NM_000110.4:c.218T>C MANE Select	NP_000101.2:p.Leu73Pro