Canonical Allele Identifier: CA1182717151
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098437G= , CM000663.2:g.97098437G= GRCh38
NC_000001.10:g.97563993G= , CM000663.1:g.97563993G= GRCh37
NC_000001.9:g.97336581G= NCBI36
NG_008807.2:g.827623C= , LRG_722:g.827623C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2766+52C= (DPYD) MANE Select ENSP00000359211.3:n.2766+52C=
ENST00000370192.7:c.2766+52C= (DPYD) ENSP00000359211.3:n.2766+52C=
NM_000110.3:c.2766+52C= , LRG_722t1:c.2766+52C= (DPYD) NP_000101.2:n.2766+52C=
NR_046590.1:n.64+2451G= (DPYD-AS1)
XM_005270562.3:c.2550+52C= (DPYD) XP_005270619.2:n.2550+52C=
XM_017000507.1:c.2655+52C= (DPYD) XP_016855996.1:n.2655+52C=
XM_017000508.2:c.2271+52C= (DPYD) XP_016855997.1:n.2271+52C=
XM_017000509.2:c.2271+52C= (DPYD) XP_016855998.1:n.2271+52C=
XM_017000510.1:c.2271+52C= (DPYD) XP_016855999.1:n.2271+52C=
NM_000110.4:c.2766+52C= (DPYD) MANE Select NP_000101.2:n.2766+52C=
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