Canonical Allele Identifier: CA525177654

Gene: DPYD

Linked Data

• dbSNP Id: rs1423842132
• gnomAD v2: 1-98015087-A-G
• gnomAD v4: 1-97549531-A-G
• MyVariant Identifiers: chr1:g.98015087A>G (hg19) ; chr1:g.97549531A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549531A>G , CM000663.2:g.97549531A>G	GRCh38
NC_000001.10:g.98015087A>G , CM000663.1:g.98015087A>G	GRCh37
NC_000001.9:g.97787675A>G	NCBI36
NG_008807.2:g.376529T>C , LRG_722:g.376529T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1524+29T>C MANE Select	ENSP00000359211.3:n.1524+29T>C
ENST00000370192.7:c.1524+29T>C	ENSP00000359211.3:n.1524+29T>C
NM_000110.3:c.1524+29T>C , LRG_722t1:c.1524+29T>C	NP_000101.2:n.1524+29T>C
XM_005270562.3:c.1524+29T>C	XP_005270619.2:n.1524+29T>C
XM_006710397.2:c.1524+29T>C	XP_006710460.1:n.1524+29T>C
XM_006710397.3:c.1524+29T>C	XP_006710460.1:n.1524+29T>C
XM_017000507.1:c.1413+29T>C	XP_016855996.1:n.1413+29T>C
XM_017000508.2:c.1029+29T>C	XP_016855997.1:n.1029+29T>C
XM_017000509.2:c.1029+29T>C	XP_016855998.1:n.1029+29T>C
XM_017000510.1:c.1029+29T>C	XP_016855999.1:n.1029+29T>C
NM_000110.4:c.1524+29T>C MANE Select	NP_000101.2:n.1524+29T>C