Canonical Allele Identifier: CA1807671447

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379557_104379561delinsCTAAG , CM000670.2:g.104379557_104379561delinsCTAAG	GRCh38
NC_000008.10:g.105391785_105391789delinsCTAAG , CM000670.1:g.105391785_105391789delinsCTAAG	GRCh37
NC_000008.9:g.105460961_105460965delinsCTAAG	NCBI36
NG_008840.1:g.92489_92493delinsCTTAG
NG_008840.2:g.92489_92493delinsCTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.*297_*301delinsCTTAG MANE Select	ENSP00000276651.2:n.*297_*301delinsCTTAG
ENST00000351513.6:c.*297_*301delinsCTTAG	ENSP00000276651.2:n.*297_*301delinsCTTAG
ENST00000520806.1:n.511_515delinsCTTAG
ENST00000521601.1:n.328+1623_328+1627delinsCTTAG
ENST00000533874.1:c.356_360delinsCTTAG
NM_001385.2:c.*297_*301delinsCTTAG	NP_001376.1:n.*297_*301delinsCTTAG
XM_005250818.2:c.*297_*301delinsCTTAG	XP_005250875.1:n.*297_*301delinsCTTAG
XM_006716518.2:c.*297_*301delinsCTTAG	XP_006716581.1:n.*297_*301delinsCTTAG
XM_005250818.3:c.*297_*301delinsCTTAG	XP_005250875.1:n.*297_*301delinsCTTAG
XM_006716518.3:c.*297_*301delinsCTTAG	XP_006716581.1:n.*297_*301delinsCTTAG
XM_024447087.1:c.*834_*838delinsCTTAG	XP_024302855.1:n.*834_*838delinsCTTAG
XR_001745489.1:n.2456_2460delinsCTTAG
XR_001745490.2:n.2348_2352delinsCTTAG
NM_001385.3:c.*297_*301delinsCTTAG MANE Select	NP_001376.1:n.*297_*301delinsCTTAG