Canonical Allele Identifier: CA1182979312
Gene: DPYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691757A= , CM000663.2:g.97691757A= GRCh38
NC_000001.10:g.98157313A= , CM000663.1:g.98157313A= GRCh37
NC_000001.9:g.97929901A= NCBI36
NG_008807.2:g.234303T= , LRG_722:g.234303T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.722T= MANE Select ENSP00000359211.3:p.Val241=
ENST00000370192.7:c.722T= ENSP00000359211.3:p.Val241=
ENST00000474241.1:n.486T=
NM_000110.3:c.722T= , LRG_722t1:c.722T= NP_000101.2:p.Val241=
XM_005270562.3:c.722T= XP_005270619.2:p.Val241=
XM_006710397.2:c.722T= XP_006710460.1:p.Val241=
XM_006710397.3:c.722T= XP_006710460.1:p.Val241=
XM_017000507.1:c.611T= XP_016855996.1:p.Val204=
XM_017000508.2:c.227T= XP_016855997.1:p.Val76=
XM_017000509.2:c.227T= XP_016855998.1:p.Val76=
XM_017000510.1:c.227T= XP_016855999.1:p.Val76=
NM_000110.4:c.722T= MANE Select NP_000101.2:p.Val241=