Canonical Allele Identifier: CA740810033

Gene: DPYD

Linked Data

• dbSNP Id: rs1271540638
• MyVariant Identifiers: chr1:g.97839037G>C (hg19) ; chr1:g.97373481G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97373481G>C , CM000663.2:g.97373481G>C	GRCh38
NC_000001.10:g.97839037G>C , CM000663.1:g.97839037G>C	GRCh37
NC_000001.9:g.97611625G>C	NCBI36
NG_008807.2:g.552579C>G , LRG_722:g.552579C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2058+80C>G MANE Select	ENSP00000359211.3:n.2058+80C>G
ENST00000370192.7:c.2058+80C>G	ENSP00000359211.3:n.2058+80C>G
NM_000110.3:c.2058+80C>G , LRG_722t1:c.2058+80C>G	NP_000101.2:n.2058+80C>G
XM_005270562.3:c.1842+80C>G	XP_005270619.2:n.1842+80C>G
XM_006710397.2:c.2058+80C>G	XP_006710460.1:n.2058+80C>G
XR_947619.1:n.1125-2047G>C
XR_947620.1:n.1124+6280G>C
XR_947621.1:n.1125-2047G>C
XM_006710397.3:c.2058+80C>G	XP_006710460.1:n.2058+80C>G
XM_017000507.1:c.1947+80C>G	XP_016855996.1:n.1947+80C>G
XM_017000508.2:c.1563+80C>G	XP_016855997.1:n.1563+80C>G
XM_017000509.2:c.1563+80C>G	XP_016855998.1:n.1563+80C>G
XM_017000510.1:c.1563+80C>G	XP_016855999.1:n.1563+80C>G
NM_000110.4:c.2058+80C>G MANE Select	NP_000101.2:n.2058+80C>G