Canonical Allele Identifier: CA341376000
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs1182668539
gnomAD v3: 1-97450102-C-T
gnomAD v4: 1-97450102-C-T
MyVariant Identifiers: chr1:g.97915658C>T (hg19) chr1:g.97450102C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97450102C>T , CM000663.2:g.97450102C>T GRCh38
NC_000001.10:g.97915658C>T , CM000663.1:g.97915658C>T GRCh37
NC_000001.9:g.97688246C>T NCBI36
NG_008807.2:g.475958G>A , LRG_722:g.475958G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.1862G>A MANE Select ENSP00000359211.3:p.Trp621Ter
ENST00000370192.7:c.1862G>A ENSP00000359211.3:p.Trp621Ter
NM_000110.3:c.1862G>A , LRG_722t1:c.1862G>A NP_000101.2:p.Trp621Ter
XM_005270562.3:c.1646G>A XP_005270619.2:p.Trp549Ter
XM_006710397.2:c.1862G>A XP_006710460.1:p.Trp621Ter
XM_006710397.3:c.1862G>A XP_006710460.1:p.Trp621Ter
XM_017000507.1:c.1751G>A XP_016855996.1:p.Trp584Ter
XM_017000508.2:c.1367G>A XP_016855997.1:p.Trp456Ter
XM_017000509.2:c.1367G>A XP_016855998.1:p.Trp456Ter
XM_017000510.1:c.1367G>A XP_016855999.1:p.Trp456Ter
NM_000110.4:c.1862G>A MANE Select NP_000101.2:p.Trp621Ter
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