Canonical Allele Identifier: CA1807671437

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379521_104379522delinsGA , CM000670.2:g.104379521_104379522delinsGA	GRCh38
NC_000008.10:g.105391749_105391750delinsGA , CM000670.1:g.105391749_105391750delinsGA	GRCh37
NC_000008.9:g.105460925_105460926delinsGA	NCBI36
NG_008840.1:g.92528_92529delinsTC
NG_008840.2:g.92528_92529delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.*336_*337delinsTC MANE Select	ENSP00000276651.2:n.*336_*337delinsTC
ENST00000351513.6:c.*336_*337delinsTC	ENSP00000276651.2:n.*336_*337delinsTC
ENST00000520806.1:n.550_551delinsTC
ENST00000521601.1:n.328+1662_328+1663delinsTC
ENST00000533874.1:c.395_396delinsTC
NM_001385.2:c.*336_*337delinsTC	NP_001376.1:n.*336_*337delinsTC
XM_005250818.2:c.*336_*337delinsTC	XP_005250875.1:n.*336_*337delinsTC
XM_006716518.2:c.*336_*337delinsTC	XP_006716581.1:n.*336_*337delinsTC
XM_005250818.3:c.*336_*337delinsTC	XP_005250875.1:n.*336_*337delinsTC
XM_006716518.3:c.*336_*337delinsTC	XP_006716581.1:n.*336_*337delinsTC
XM_024447087.1:c.*873_*874delinsTC	XP_024302855.1:n.*873_*874delinsTC
XR_001745489.1:n.2495_2496delinsTC
XR_001745490.2:n.2387_2388delinsTC
NM_001385.3:c.*336_*337delinsTC MANE Select	NP_001376.1:n.*336_*337delinsTC