Canonical Allele Identifier: CA2646706219
Gene: DPYD HGNC NCBI

Linked Data

gnomAD v4: 1-97549519-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549519C>G , CM000663.2:g.97549519C>G GRCh38
NC_000001.10:g.98015075C>G , CM000663.1:g.98015075C>G GRCh37
NC_000001.9:g.97787663C>G NCBI36
NG_008807.2:g.376541G>C , LRG_722:g.376541G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.1524+41G>C MANE Select ENSP00000359211.3:n.1524+41G>C
ENST00000370192.7:c.1524+41G>C ENSP00000359211.3:n.1524+41G>C
NM_000110.3:c.1524+41G>C , LRG_722t1:c.1524+41G>C NP_000101.2:n.1524+41G>C
XM_005270562.3:c.1524+41G>C XP_005270619.2:n.1524+41G>C
XM_006710397.2:c.1524+41G>C XP_006710460.1:n.1524+41G>C
XM_006710397.3:c.1524+41G>C XP_006710460.1:n.1524+41G>C
XM_017000507.1:c.1413+41G>C XP_016855996.1:n.1413+41G>C
XM_017000508.2:c.1029+41G>C XP_016855997.1:n.1029+41G>C
XM_017000509.2:c.1029+41G>C XP_016855998.1:n.1029+41G>C
XM_017000510.1:c.1029+41G>C XP_016855999.1:n.1029+41G>C
NM_000110.4:c.1524+41G>C MANE Select NP_000101.2:n.1524+41G>C
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