Canonical Allele Identifier: CA341379384

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.98293677C>T (hg19) ; chr1:g.97828121C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828121C>T , CM000663.2:g.97828121C>T	GRCh38
NC_000001.10:g.98293677C>T , CM000663.1:g.98293677C>T	GRCh37
NC_000001.9:g.98066265C>T	NCBI36
NG_008807.2:g.97939G>A , LRG_722:g.97939G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.226G>A MANE Select	ENSP00000359211.3:p.Ala76Thr
ENST00000306031.5:c.226G>A	ENSP00000307107.5:p.Ala76Thr
ENST00000370192.7:c.226G>A	ENSP00000359211.3:p.Ala76Thr
NM_000110.3:c.226G>A , LRG_722t1:c.226G>A	NP_000101.2:p.Ala76Thr
NM_001160301.1:c.226G>A , LRG_722t2:c.226G>A	NP_001153773.1:p.Ala76Thr
XM_005270562.3:c.226G>A	XP_005270619.2:p.Ala76Thr
XM_006710397.2:c.226G>A	XP_006710460.1:p.Ala76Thr
XM_006710397.3:c.226G>A	XP_006710460.1:p.Ala76Thr
XM_017000507.1:c.115G>A	XP_016855996.1:p.Ala39Thr
XM_017000508.2:c.-485G>A	XP_016855997.1:n.-485G>A
XM_017000509.2:c.-383G>A	XP_016855998.1:n.-383G>A
XM_017000510.1:c.-383G>A	XP_016855999.1:n.-383G>A
XR_001737014.1:n.363G>A
NM_000110.4:c.226G>A MANE Select	NP_000101.2:p.Ala76Thr