Canonical Allele Identifier: CA1807671444

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379532A= , CM000670.2:g.104379532A=	GRCh38
NC_000008.10:g.105391760A= , CM000670.1:g.105391760A=	GRCh37
NC_000008.9:g.105460936A=	NCBI36
NG_008840.1:g.92518T=
NG_008840.2:g.92518T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.*326T= MANE Select	ENSP00000276651.2:n.*326T=
ENST00000351513.6:c.*326T=	ENSP00000276651.2:n.*326T=
ENST00000520806.1:n.540T=
ENST00000521601.1:n.328+1652T=
ENST00000533874.1:c.385T=
NM_001385.2:c.*326T=	NP_001376.1:n.*326T=
XM_005250818.2:c.*326T=	XP_005250875.1:n.*326T=
XM_006716518.2:c.*326T=	XP_006716581.1:n.*326T=
XM_005250818.3:c.*326T=	XP_005250875.1:n.*326T=
XM_006716518.3:c.*326T=	XP_006716581.1:n.*326T=
XM_024447087.1:c.*863T=	XP_024302855.1:n.*863T=
XR_001745489.1:n.2485T=
XR_001745490.2:n.2377T=
NM_001385.3:c.*326T= MANE Select	NP_001376.1:n.*326T=