Canonical Allele Identifier: CA1807671442

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379525_104379529delinsCTATT , CM000670.2:g.104379525_104379529delinsCTATT	GRCh38
NC_000008.10:g.105391753_105391757delinsCTATT , CM000670.1:g.105391753_105391757delinsCTATT	GRCh37
NC_000008.9:g.105460929_105460933delinsCTATT	NCBI36
NG_008840.1:g.92521_92525delinsAATAG
NG_008840.2:g.92521_92525delinsAATAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.*329_*333delinsAATAG MANE Select	ENSP00000276651.2:n.*329_*333delinsAATAG
ENST00000351513.6:c.*329_*333delinsAATAG	ENSP00000276651.2:n.*329_*333delinsAATAG
ENST00000520806.1:n.543_547delinsAATAG
ENST00000521601.1:n.328+1655_328+1659delinsAATAG
ENST00000533874.1:c.388_392delinsAATAG
NM_001385.2:c.*329_*333delinsAATAG	NP_001376.1:n.*329_*333delinsAATAG
XM_005250818.2:c.*329_*333delinsAATAG	XP_005250875.1:n.*329_*333delinsAATAG
XM_006716518.2:c.*329_*333delinsAATAG	XP_006716581.1:n.*329_*333delinsAATAG
XM_005250818.3:c.*329_*333delinsAATAG	XP_005250875.1:n.*329_*333delinsAATAG
XM_006716518.3:c.*329_*333delinsAATAG	XP_006716581.1:n.*329_*333delinsAATAG
XM_024447087.1:c.*866_*870delinsAATAG	XP_024302855.1:n.*866_*870delinsAATAG
XR_001745489.1:n.2488_2492delinsAATAG
XR_001745490.2:n.2380_2384delinsAATAG
NM_001385.3:c.*329_*333delinsAATAG MANE Select	NP_001376.1:n.*329_*333delinsAATAG