Canonical Allele Identifier: CA27638125

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97515787A>T , CM000663.2:g.97515787A>T	GRCh38
NC_000001.10:g.97981343A>T , CM000663.1:g.97981343A>T	GRCh37
NC_000001.9:g.97753931A>T	NCBI36
NG_008807.2:g.410273T>A , LRG_722:g.410273T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000110.4:c.1679T>A MANE Select	NP_000101.2:p.Ile560Asn
ENST00000370192.8:c.1679T>A MANE Select	ENSP00000359211.3:p.Ile560Asn
NM_000110.3:c.1679T>A , LRG_722t1:c.1679T>A	NP_000101.2:p.Ile560Asn
ENST00000370192.7:c.1679T>A	ENSP00000359211.3:p.Ile560Asn
XM_005270562.3:c.1524+33773T>A	XP_005270619.2:n.1524+33773T>A
XM_006710397.2:c.1679T>A	XP_006710460.1:p.Ile560Asn
XM_006710397.3:c.1679T>A	XP_006710460.1:p.Ile560Asn
XM_017000507.1:c.1568T>A	XP_016855996.1:p.Ile523Asn
XM_017000508.2:c.1184T>A	XP_016855997.1:p.Ile395Asn
XM_017000509.2:c.1184T>A	XP_016855998.1:p.Ile395Asn
XM_017000510.1:c.1184T>A	XP_016855999.1:p.Ile395Asn