Canonical Allele Identifier: CA1182979286
Gene: DPYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691681T= , CM000663.2:g.97691681T= GRCh38
NC_000001.10:g.98157237T= , CM000663.1:g.98157237T= GRCh37
NC_000001.9:g.97929825T= NCBI36
NG_008807.2:g.234379A= , LRG_722:g.234379A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.762+36A= MANE Select ENSP00000359211.3:n.762+36A=
ENST00000370192.7:c.762+36A= ENSP00000359211.3:n.762+36A=
ENST00000474241.1:n.562A=
NM_000110.3:c.762+36A= , LRG_722t1:c.762+36A= NP_000101.2:n.762+36A=
XM_005270562.3:c.762+36A= XP_005270619.2:n.762+36A=
XM_006710397.2:c.762+36A= XP_006710460.1:n.762+36A=
XM_006710397.3:c.762+36A= XP_006710460.1:n.762+36A=
XM_017000507.1:c.651+36A= XP_016855996.1:n.651+36A=
XM_017000508.2:c.267+36A= XP_016855997.1:n.267+36A=
XM_017000509.2:c.267+36A= XP_016855998.1:n.267+36A=
XM_017000510.1:c.267+36A= XP_016855999.1:n.267+36A=
NM_000110.4:c.762+36A= MANE Select NP_000101.2:n.762+36A=