Canonical Allele Identifier: CA341373874

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97079071C>T , CM000663.2:g.97079071C>T	GRCh38
NC_000001.10:g.97544627C>T , CM000663.1:g.97544627C>T	GRCh37
NC_000001.9:g.97317215C>T	NCBI36
NG_008807.2:g.846989G>A , LRG_722:g.846989G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000110.4:c.2983G>A MANE Select	NP_000101.2:p.Val995Ile
ENST00000370192.8:c.2983G>A MANE Select	ENSP00000359211.3:p.Val995Ile
NM_000110.3:c.2983G>A , LRG_722t1:c.2983G>A	NP_000101.2:p.Val995Ile
ENST00000370192.7:c.2983G>A	ENSP00000359211.3:p.Val995Ile
XM_005270562.3:c.2767G>A	XP_005270619.2:p.Val923Ile
XM_017000507.1:c.2872G>A	XP_016855996.1:p.Val958Ile
XM_017000508.2:c.2488G>A	XP_016855997.1:p.Val830Ile
XM_017000509.2:c.2488G>A	XP_016855998.1:p.Val830Ile
XM_017000510.1:c.2488G>A	XP_016855999.1:p.Val830Ile