Canonical Allele Identifier: CA1004794328

Gene: DPYD

Linked Data

• dbSNP Id: rs1194863133
• gnomAD v3: 1-97691254-A-C
• gnomAD v4: 1-97691254-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691254A>C , CM000663.2:g.97691254A>C	GRCh38
NC_000001.10:g.98156810A>C , CM000663.1:g.98156810A>C	GRCh37
NC_000001.9:g.97929398A>C	NCBI36
NG_008807.2:g.234806T>G , LRG_722:g.234806T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+463T>G MANE Select	ENSP00000359211.3:n.762+463T>G
ENST00000370192.7:c.762+463T>G	ENSP00000359211.3:n.762+463T>G
ENST00000474241.1:n.989T>G
NM_000110.3:c.762+463T>G , LRG_722t1:c.762+463T>G	NP_000101.2:n.762+463T>G
XM_005270562.3:c.762+463T>G	XP_005270619.2:n.762+463T>G
XM_006710397.2:c.762+463T>G	XP_006710460.1:n.762+463T>G
XM_006710397.3:c.762+463T>G	XP_006710460.1:n.762+463T>G
XM_017000507.1:c.651+463T>G	XP_016855996.1:n.651+463T>G
XM_017000508.2:c.267+463T>G	XP_016855997.1:n.267+463T>G
XM_017000509.2:c.267+463T>G	XP_016855998.1:n.267+463T>G
XM_017000510.1:c.267+463T>G	XP_016855999.1:n.267+463T>G
NM_000110.4:c.762+463T>G MANE Select	NP_000101.2:n.762+463T>G