Canonical Allele Identifier: CA1182736746
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97144470G>A , CM000663.2:g.97144470G>A GRCh38
NC_000001.10:g.97610026G>A , CM000663.1:g.97610026G>A GRCh37
NC_000001.9:g.97382614G>A NCBI36
NG_008807.2:g.781590C>T , LRG_722:g.781590C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2623-45838C>T (DPYD) MANE Select ENSP00000359211.3:n.2623-45838C>T
ENST00000370192.7:c.2623-45838C>T (DPYD) ENSP00000359211.3:n.2623-45838C>T
NM_000110.3:c.2623-45838C>T , LRG_722t1:c.2623-45838C>T (DPYD) NP_000101.2:n.2623-45838C>T
NR_046590.1:n.64+48484G>A (DPYD-AS1)
XM_005270562.3:c.2407-45838C>T (DPYD) XP_005270619.2:n.2407-45838C>T
XM_017000507.1:c.2512-45838C>T (DPYD) XP_016855996.1:n.2512-45838C>T
XM_017000508.2:c.2128-45838C>T (DPYD) XP_016855997.1:n.2128-45838C>T
XM_017000509.2:c.2128-45838C>T (DPYD) XP_016855998.1:n.2128-45838C>T
XM_017000510.1:c.2128-45838C>T (DPYD) XP_016855999.1:n.2128-45838C>T
NM_000110.4:c.2623-45838C>T (DPYD) MANE Select NP_000101.2:n.2623-45838C>T
Search 100 bp 5'
Search 100 bp 3'