Canonical Allele Identifier: CA341373541

Gene: DPYD DPYD-AS1

Linked Data

• COSMIC: COSM6258773
• MyVariant Identifiers: chr1:g.97658752G>T (hg19) ; chr1:g.97193196G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193196G>T , CM000663.2:g.97193196G>T	GRCh38
NC_000001.10:g.97658752G>T , CM000663.1:g.97658752G>T	GRCh37
NC_000001.9:g.97431340G>T	NCBI36
NG_008807.2:g.732864C>A , LRG_722:g.732864C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2495C>A (DPYD) MANE Select	ENSP00000359211.3:p.Thr832Asn
ENST00000370192.7:c.2495C>A (DPYD)	ENSP00000359211.3:p.Thr832Asn
NM_000110.3:c.2495C>A , LRG_722t1:c.2495C>A (DPYD)	NP_000101.2:p.Thr832Asn
NR_046590.1:n.65-72218G>T (DPYD-AS1)
XM_005270562.3:c.2279C>A (DPYD)	XP_005270619.2:p.Thr760Asn
XM_006710397.2:c.2495C>A (DPYD)	XP_006710460.1:p.Thr832Asn
XM_006710397.3:c.2495C>A (DPYD)	XP_006710460.1:p.Thr832Asn
XM_017000507.1:c.2384C>A (DPYD)	XP_016855996.1:p.Thr795Asn
XM_017000508.2:c.2000C>A (DPYD)	XP_016855997.1:p.Thr667Asn
XM_017000509.2:c.2000C>A (DPYD)	XP_016855998.1:p.Thr667Asn
XM_017000510.1:c.2000C>A (DPYD)	XP_016855999.1:p.Thr667Asn
NM_000110.4:c.2495C>A (DPYD) MANE Select	NP_000101.2:p.Thr832Asn