Canonical Allele Identifier: CA1182717148
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098426T= , CM000663.2:g.97098426T= GRCh38
NC_000001.10:g.97563982T= , CM000663.1:g.97563982T= GRCh37
NC_000001.9:g.97336570T= NCBI36
NG_008807.2:g.827634A= , LRG_722:g.827634A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2766+63A= (DPYD) MANE Select ENSP00000359211.3:n.2766+63A=
ENST00000370192.7:c.2766+63A= (DPYD) ENSP00000359211.3:n.2766+63A=
NM_000110.3:c.2766+63A= , LRG_722t1:c.2766+63A= (DPYD) NP_000101.2:n.2766+63A=
NR_046590.1:n.64+2440T= (DPYD-AS1)
XM_005270562.3:c.2550+63A= (DPYD) XP_005270619.2:n.2550+63A=
XM_017000507.1:c.2655+63A= (DPYD) XP_016855996.1:n.2655+63A=
XM_017000508.2:c.2271+63A= (DPYD) XP_016855997.1:n.2271+63A=
XM_017000509.2:c.2271+63A= (DPYD) XP_016855998.1:n.2271+63A=
XM_017000510.1:c.2271+63A= (DPYD) XP_016855999.1:n.2271+63A=
NM_000110.4:c.2766+63A= (DPYD) MANE Select NP_000101.2:n.2766+63A=
Search 100 bp 5'
Search 100 bp 3'