Canonical Allele Identifier: CA524790375
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs1247255465
gnomAD v2: 1-98157266-C-T
gnomAD v4: 1-97691710-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691710C>T , CM000663.2:g.97691710C>T GRCh38
NC_000001.10:g.98157266C>T , CM000663.1:g.98157266C>T GRCh37
NC_000001.9:g.97929854C>T NCBI36
NG_008807.2:g.234350G>A , LRG_722:g.234350G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.762+7G>A MANE Select ENSP00000359211.3:n.762+7G>A
ENST00000370192.7:c.762+7G>A ENSP00000359211.3:n.762+7G>A
ENST00000474241.1:n.533G>A
NM_000110.3:c.762+7G>A , LRG_722t1:c.762+7G>A NP_000101.2:n.762+7G>A
XM_005270562.3:c.762+7G>A XP_005270619.2:n.762+7G>A
XM_006710397.2:c.762+7G>A XP_006710460.1:n.762+7G>A
XM_006710397.3:c.762+7G>A XP_006710460.1:n.762+7G>A
XM_017000507.1:c.651+7G>A XP_016855996.1:n.651+7G>A
XM_017000508.2:c.267+7G>A XP_016855997.1:n.267+7G>A
XM_017000509.2:c.267+7G>A XP_016855998.1:n.267+7G>A
XM_017000510.1:c.267+7G>A XP_016855999.1:n.267+7G>A
NM_000110.4:c.762+7G>A MANE Select NP_000101.2:n.762+7G>A