Canonical Allele Identifier: CA341379407

Gene: DPYD

Linked Data

• dbSNP Id: rs1571426976
• gnomAD v4: 1-97828133-C-T
• MyVariant Identifiers: chr1:g.98293689C>T (hg19) ; chr1:g.97828133C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828133C>T , CM000663.2:g.97828133C>T	GRCh38
NC_000001.10:g.98293689C>T , CM000663.1:g.98293689C>T	GRCh37
NC_000001.9:g.98066277C>T	NCBI36
NG_008807.2:g.97927G>A , LRG_722:g.97927G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.214G>A MANE Select	ENSP00000359211.3:p.Ala72Thr
ENST00000306031.5:c.214G>A	ENSP00000307107.5:p.Ala72Thr
ENST00000370192.7:c.214G>A	ENSP00000359211.3:p.Ala72Thr
NM_000110.3:c.214G>A , LRG_722t1:c.214G>A	NP_000101.2:p.Ala72Thr
NM_001160301.1:c.214G>A , LRG_722t2:c.214G>A	NP_001153773.1:p.Ala72Thr
XM_005270562.3:c.214G>A	XP_005270619.2:p.Ala72Thr
XM_006710397.2:c.214G>A	XP_006710460.1:p.Ala72Thr
XM_006710397.3:c.214G>A	XP_006710460.1:p.Ala72Thr
XM_017000507.1:c.103G>A	XP_016855996.1:p.Ala35Thr
XM_017000508.2:c.-497G>A	XP_016855997.1:n.-497G>A
XM_017000509.2:c.-395G>A	XP_016855998.1:n.-395G>A
XM_017000510.1:c.-395G>A	XP_016855999.1:n.-395G>A
XR_001737014.1:n.351G>A
NM_000110.4:c.214G>A MANE Select	NP_000101.2:p.Ala72Thr