Canonical Allele Identifier: CA740795484

Gene: DPYD

Linked Data

• dbSNP Id: rs1257862851
• gnomAD v4: 1-97549530-A-C
• MyVariant Identifiers: chr1:g.98015086A>C (hg19) ; chr1:g.97549530A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549530A>C , CM000663.2:g.97549530A>C	GRCh38
NC_000001.10:g.98015086A>C , CM000663.1:g.98015086A>C	GRCh37
NC_000001.9:g.97787674A>C	NCBI36
NG_008807.2:g.376530T>G , LRG_722:g.376530T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1524+30T>G MANE Select	ENSP00000359211.3:n.1524+30T>G
ENST00000370192.7:c.1524+30T>G	ENSP00000359211.3:n.1524+30T>G
NM_000110.3:c.1524+30T>G , LRG_722t1:c.1524+30T>G	NP_000101.2:n.1524+30T>G
XM_005270562.3:c.1524+30T>G	XP_005270619.2:n.1524+30T>G
XM_006710397.2:c.1524+30T>G	XP_006710460.1:n.1524+30T>G
XM_006710397.3:c.1524+30T>G	XP_006710460.1:n.1524+30T>G
XM_017000507.1:c.1413+30T>G	XP_016855996.1:n.1413+30T>G
XM_017000508.2:c.1029+30T>G	XP_016855997.1:n.1029+30T>G
XM_017000509.2:c.1029+30T>G	XP_016855998.1:n.1029+30T>G
XM_017000510.1:c.1029+30T>G	XP_016855999.1:n.1029+30T>G
NM_000110.4:c.1524+30T>G MANE Select	NP_000101.2:n.1524+30T>G