Canonical Allele Identifier: CA2696708552
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs2102181383
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97573702A>T , CM000663.2:g.97573702A>T GRCh38
NC_000001.10:g.98039258A>T , CM000663.1:g.98039258A>T GRCh37
NC_000001.9:g.97811846A>T NCBI36
NG_008807.2:g.352358T>A , LRG_722:g.352358T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.1339+58T>A MANE Select ENSP00000359211.3:n.1339+58T>A
ENST00000370192.7:c.1339+58T>A ENSP00000359211.3:n.1339+58T>A
NM_000110.3:c.1339+58T>A , LRG_722t1:c.1339+58T>A NP_000101.2:n.1339+58T>A
XM_005270562.3:c.1339+58T>A XP_005270619.2:n.1339+58T>A
XM_006710397.2:c.1339+58T>A XP_006710460.1:n.1339+58T>A
XM_006710397.3:c.1339+58T>A XP_006710460.1:n.1339+58T>A
XM_017000507.1:c.1228+58T>A XP_016855996.1:n.1228+58T>A
XM_017000508.2:c.844+58T>A XP_016855997.1:n.844+58T>A
XM_017000509.2:c.844+58T>A XP_016855998.1:n.844+58T>A
XM_017000510.1:c.844+58T>A XP_016855999.1:n.844+58T>A
NM_000110.4:c.1339+58T>A MANE Select NP_000101.2:n.1339+58T>A
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