Canonical Allele Identifier: CA341377454

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.98015147T>A (hg19) ; chr1:g.97549591T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549591T>A , CM000663.2:g.97549591T>A	GRCh38
NC_000001.10:g.98015147T>A , CM000663.1:g.98015147T>A	GRCh37
NC_000001.9:g.97787735T>A	NCBI36
NG_008807.2:g.376469A>T , LRG_722:g.376469A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1493A>T MANE Select	ENSP00000359211.3:p.Gln498Leu
ENST00000370192.7:c.1493A>T	ENSP00000359211.3:p.Gln498Leu
NM_000110.3:c.1493A>T , LRG_722t1:c.1493A>T	NP_000101.2:p.Gln498Leu
XM_005270562.3:c.1493A>T	XP_005270619.2:p.Gln498Leu
XM_006710397.2:c.1493A>T	XP_006710460.1:p.Gln498Leu
XM_006710397.3:c.1493A>T	XP_006710460.1:p.Gln498Leu
XM_017000507.1:c.1382A>T	XP_016855996.1:p.Gln461Leu
XM_017000508.2:c.998A>T	XP_016855997.1:p.Gln333Leu
XM_017000509.2:c.998A>T	XP_016855998.1:p.Gln333Leu
XM_017000510.1:c.998A>T	XP_016855999.1:p.Gln333Leu
NM_000110.4:c.1493A>T MANE Select	NP_000101.2:p.Gln498Leu