Canonical Allele Identifier: CA2688213211

Gene: DPYS

Linked Data

• gnomAD v4: 8-104379594-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379597del , CM000670.2:g.104379597del	GRCh38
NC_000008.10:g.105391825del , CM000670.1:g.105391825del	GRCh37
NC_000008.9:g.105461001del	NCBI36
NG_008840.1:g.92455del
NG_008840.2:g.92455del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.*263del MANE Select	ENSP00000276651.2:n.*263del
ENST00000351513.6:c.*263del	ENSP00000276651.2:n.*263del
ENST00000520806.1:n.477del
ENST00000521601.1:n.328+1589del
ENST00000533874.1:c.322del
NM_001385.2:c.*263del	NP_001376.1:n.*263del
XM_005250818.2:c.*263del	XP_005250875.1:n.*263del
XM_006716518.2:c.*263del	XP_006716581.1:n.*263del
XM_005250818.3:c.*263del	XP_005250875.1:n.*263del
XM_006716518.3:c.*263del	XP_006716581.1:n.*263del
XM_024447087.1:c.*800del	XP_024302855.1:n.*800del
XR_001745489.1:n.2422del
XR_001745490.2:n.2314del
NM_001385.3:c.*263del MANE Select	NP_001376.1:n.*263del