Canonical Allele Identifier: CA27502978

Gene: DPYD

Linked Data

• dbSNP Id: rs753791428
• MyVariant Identifiers: chr1:g.97926880C>G (hg19) ; chr1:g.97461324C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97461324C>G , CM000663.2:g.97461324C>G	GRCh38
NC_000001.10:g.97926880C>G , CM000663.1:g.97926880C>G	GRCh37
NC_000001.9:g.97699468C>G	NCBI36
NG_008807.2:g.464736G>C , LRG_722:g.464736G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1741-11101G>C MANE Select	ENSP00000359211.3:n.1741-11101G>C
ENST00000370192.7:c.1741-11101G>C	ENSP00000359211.3:n.1741-11101G>C
NM_000110.3:c.1741-11101G>C , LRG_722t1:c.1741-11101G>C	NP_000101.2:n.1741-11101G>C
XM_005270562.3:c.1525-11101G>C	XP_005270619.2:n.1525-11101G>C
XM_006710397.2:c.1741-11101G>C	XP_006710460.1:n.1741-11101G>C
XM_006710397.3:c.1741-11101G>C	XP_006710460.1:n.1741-11101G>C
XM_017000507.1:c.1630-11101G>C	XP_016855996.1:n.1630-11101G>C
XM_017000508.2:c.1246-11101G>C	XP_016855997.1:n.1246-11101G>C
XM_017000509.2:c.1246-11101G>C	XP_016855998.1:n.1246-11101G>C
XM_017000510.1:c.1246-11101G>C	XP_016855999.1:n.1246-11101G>C
NM_000110.4:c.1741-11101G>C MANE Select	NP_000101.2:n.1741-11101G>C