Canonical Allele Identifier: CA2695198095

Gene: DPYD

Linked Data

• ClinVar Variation Id: 2674934
• ClinVar RCV Id: RCV003467847

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828127_97828134delinsATTG , CM000663.2:g.97828127_97828134delinsATTG	GRCh38
NC_000001.10:g.98293683_98293690delinsATTG , CM000663.1:g.98293683_98293690delinsATTG	GRCh37
NC_000001.9:g.98066271_98066278delinsATTG	NCBI36
NG_008807.2:g.97926_97933delinsCAAT , LRG_722:g.97926_97933delinsCAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.213_220delinsCAAT MANE Select	ENSP00000359211.3:p.Ala72AsnfsTer5
ENST00000306031.5:c.213_220delinsCAAT	ENSP00000307107.5:p.Ala72AsnfsTer5
ENST00000370192.7:c.213_220delinsCAAT	ENSP00000359211.3:p.Ala72AsnfsTer5
NM_000110.3:c.213_220delinsCAAT , LRG_722t1:c.213_220delinsCAAT	NP_000101.2:p.Ala72AsnfsTer5
NM_001160301.1:c.213_220delinsCAAT , LRG_722t2:c.213_220delinsCAAT	NP_001153773.1:p.Ala72AsnfsTer5
XM_005270562.3:c.213_220delinsCAAT	XP_005270619.2:p.Ala72AsnfsTer5
XM_006710397.2:c.213_220delinsCAAT	XP_006710460.1:p.Ala72AsnfsTer5
XM_006710397.3:c.213_220delinsCAAT	XP_006710460.1:p.Ala72AsnfsTer5
XM_017000507.1:c.102_109delinsCAAT	XP_016855996.1:p.Ala35AsnfsTer5
XM_017000508.2:c.-498_-491delinsCAAT	XP_016855997.1:n.-498_-491delinsCAAT
XM_017000509.2:c.-396_-389delinsCAAT	XP_016855998.1:n.-396_-389delinsCAAT
XM_017000510.1:c.-396_-389delinsCAAT	XP_016855999.1:n.-396_-389delinsCAAT
XR_001737014.1:n.350_357delinsCAAT
NM_000110.4:c.213_220delinsCAAT MANE Select	NP_000101.2:p.Ala72AsnfsTer5