Canonical Allele Identifier: CA341379174
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs1057517065
gnomAD v2: 1-98157271-A-T
gnomAD v4: 1-97691715-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691715A>T , CM000663.2:g.97691715A>T GRCh38
NC_000001.10:g.98157271A>T , CM000663.1:g.98157271A>T GRCh37
NC_000001.9:g.97929859A>T NCBI36
NG_008807.2:g.234345T>A , LRG_722:g.234345T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.762+2T>A MANE Select ENSP00000359211.3:n.762+2T>A
ENST00000370192.7:c.762+2T>A ENSP00000359211.3:n.762+2T>A
ENST00000474241.1:n.528T>A
NM_000110.3:c.762+2T>A , LRG_722t1:c.762+2T>A NP_000101.2:n.762+2T>A
XM_005270562.3:c.762+2T>A XP_005270619.2:n.762+2T>A
XM_006710397.2:c.762+2T>A XP_006710460.1:n.762+2T>A
XM_006710397.3:c.762+2T>A XP_006710460.1:n.762+2T>A
XM_017000507.1:c.651+2T>A XP_016855996.1:n.651+2T>A
XM_017000508.2:c.267+2T>A XP_016855997.1:n.267+2T>A
XM_017000509.2:c.267+2T>A XP_016855998.1:n.267+2T>A
XM_017000510.1:c.267+2T>A XP_016855999.1:n.267+2T>A
NM_000110.4:c.762+2T>A MANE Select NP_000101.2:n.762+2T>A