Canonical Allele Identifier: CA341379405

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.98293689C>A (hg19) ; chr1:g.97828133C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.214G>T MANE Select	ENSP00000359211.3:p.Ala72Ser
ENST00000306031.5:c.214G>T	ENSP00000307107.5:p.Ala72Ser
ENST00000370192.7:c.214G>T	ENSP00000359211.3:p.Ala72Ser
NM_000110.3:c.214G>T , LRG_722t1:c.214G>T	NP_000101.2:p.Ala72Ser
NM_001160301.1:c.214G>T , LRG_722t2:c.214G>T	NP_001153773.1:p.Ala72Ser
XM_005270562.3:c.214G>T	XP_005270619.2:p.Ala72Ser
XM_006710397.2:c.214G>T	XP_006710460.1:p.Ala72Ser
XM_006710397.3:c.214G>T	XP_006710460.1:p.Ala72Ser
XM_017000507.1:c.103G>T	XP_016855996.1:p.Ala35Ser
XM_017000508.2:c.-497G>T	XP_016855997.1:n.-497G>T
XM_017000509.2:c.-395G>T	XP_016855998.1:n.-395G>T
XM_017000510.1:c.-395G>T	XP_016855999.1:n.-395G>T
XR_001737014.1:n.351G>T
NM_000110.4:c.214G>T MANE Select	NP_000101.2:p.Ala72Ser