Canonical Allele Identifier: CA341379308
Gene: DPYD HGNC NCBI

Linked Data

gnomAD v4: 1-97691777-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691777G>C , CM000663.2:g.97691777G>C GRCh38
NC_000001.10:g.98157333G>C , CM000663.1:g.98157333G>C GRCh37
NC_000001.9:g.97929921G>C NCBI36
NG_008807.2:g.234283C>G , LRG_722:g.234283C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.702C>G MANE Select ENSP00000359211.3:p.Phe234Leu
ENST00000370192.7:c.702C>G ENSP00000359211.3:p.Phe234Leu
ENST00000474241.1:n.466C>G
NM_000110.3:c.702C>G , LRG_722t1:c.702C>G NP_000101.2:p.Phe234Leu
XM_005270562.3:c.702C>G XP_005270619.2:p.Phe234Leu
XM_006710397.2:c.702C>G XP_006710460.1:p.Phe234Leu
XM_006710397.3:c.702C>G XP_006710460.1:p.Phe234Leu
XM_017000507.1:c.591C>G XP_016855996.1:p.Phe197Leu
XM_017000508.2:c.207C>G XP_016855997.1:p.Phe69Leu
XM_017000509.2:c.207C>G XP_016855998.1:p.Phe69Leu
XM_017000510.1:c.207C>G XP_016855999.1:p.Phe69Leu
NM_000110.4:c.702C>G MANE Select NP_000101.2:p.Phe234Leu