Canonical Allele Identifier: CA963350
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs774799003
gnomAD v2: 1-98015244-G-A
gnomAD v3: 1-97549688-G-A
gnomAD v4: 1-97549688-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549688G>A , CM000663.2:g.97549688G>A GRCh38
NC_000001.10:g.98015244G>A , CM000663.1:g.98015244G>A GRCh37
NC_000001.9:g.97787832G>A NCBI36
NG_008807.2:g.376372C>T , LRG_722:g.376372C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1396C>T MANE Select ENSP00000359211.3:p.Pro466Ser
ENST00000370192.7:c.1396C>T ENSP00000359211.3:p.Pro466Ser
NM_000110.3:c.1396C>T , LRG_722t1:c.1396C>T NP_000101.2:p.Pro466Ser
XM_005270562.3:c.1396C>T XP_005270619.2:p.Pro466Ser
XM_006710397.2:c.1396C>T XP_006710460.1:p.Pro466Ser
XM_006710397.3:c.1396C>T XP_006710460.1:p.Pro466Ser
XM_017000507.1:c.1285C>T XP_016855996.1:p.Pro429Ser
XM_017000508.2:c.901C>T XP_016855997.1:p.Pro301Ser
XM_017000509.2:c.901C>T XP_016855998.1:p.Pro301Ser
XM_017000510.1:c.901C>T XP_016855999.1:p.Pro301Ser
NM_000110.4:c.1396C>T MANE Select NP_000101.2:p.Pro466Ser