Canonical Allele Identifier: CA2646703356
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

gnomAD v4: 1-97098407-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098407A>C , CM000663.2:g.97098407A>C GRCh38
NC_000001.10:g.97563963A>C , CM000663.1:g.97563963A>C GRCh37
NC_000001.9:g.97336551A>C NCBI36
NG_008807.2:g.827653T>G , LRG_722:g.827653T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2766+82T>G (DPYD) MANE Select ENSP00000359211.3:n.2766+82T>G
ENST00000370192.7:c.2766+82T>G (DPYD) ENSP00000359211.3:n.2766+82T>G
NM_000110.3:c.2766+82T>G , LRG_722t1:c.2766+82T>G (DPYD) NP_000101.2:n.2766+82T>G
NR_046590.1:n.64+2421A>C (DPYD-AS1)
XM_005270562.3:c.2550+82T>G (DPYD) XP_005270619.2:n.2550+82T>G
XM_017000507.1:c.2655+82T>G (DPYD) XP_016855996.1:n.2655+82T>G
XM_017000508.2:c.2271+82T>G (DPYD) XP_016855997.1:n.2271+82T>G
XM_017000509.2:c.2271+82T>G (DPYD) XP_016855998.1:n.2271+82T>G
XM_017000510.1:c.2271+82T>G (DPYD) XP_016855999.1:n.2271+82T>G
NM_000110.4:c.2766+82T>G (DPYD) MANE Select NP_000101.2:n.2766+82T>G
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