Canonical Allele Identifier: CA341375745
Gene: DPYD HGNC NCBI

Linked Data

gnomAD v4: 1-97382401-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97382401T>G , CM000663.2:g.97382401T>G GRCh38
NC_000001.10:g.97847957T>G , CM000663.1:g.97847957T>G GRCh37
NC_000001.9:g.97620545T>G NCBI36
NG_008807.2:g.543659A>C , LRG_722:g.543659A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1966A>C MANE Select ENSP00000359211.3:p.Lys656Gln
ENST00000370192.7:c.1966A>C ENSP00000359211.3:p.Lys656Gln
NM_000110.3:c.1966A>C , LRG_722t1:c.1966A>C NP_000101.2:p.Lys656Gln
XM_005270562.3:c.1750A>C XP_005270619.2:p.Lys584Gln
XM_006710397.2:c.1966A>C XP_006710460.1:p.Lys656Gln
XR_947619.1:n.1347-1233T>G
XR_947620.1:n.1125-1233T>G
XR_947621.1:n.1347-1233T>G
XM_006710397.3:c.1966A>C XP_006710460.1:p.Lys656Gln
XM_017000507.1:c.1855A>C XP_016855996.1:p.Lys619Gln
XM_017000508.2:c.1471A>C XP_016855997.1:p.Lys491Gln
XM_017000509.2:c.1471A>C XP_016855998.1:p.Lys491Gln
XM_017000510.1:c.1471A>C XP_016855999.1:p.Lys491Gln
XR_001737686.2:n.692-1233T>G
XR_001737687.1:n.692-1233T>G
XR_001737688.2:n.692-1233T>G
NM_000110.4:c.1966A>C MANE Select NP_000101.2:p.Lys656Gln