Canonical Allele Identifier: CA1807707808

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104466949C= , CM000670.2:g.104466949C=	GRCh38
NC_000008.10:g.105479177C= , CM000670.1:g.105479177C=	GRCh37
NC_000008.9:g.105548353C=	NCBI36
NG_008840.1:g.5101G=
NG_008840.2:g.5101G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.-29G= MANE Select	ENSP00000276651.2:n.-29G=
ENST00000351513.6:c.-29G=	ENSP00000276651.2:n.-29G=
ENST00000521573.2:c.-29G=	ENSP00000430246.2:n.-29G=
NM_001385.2:c.-29G=	NP_001376.1:n.-29G=
XM_005250818.2:c.-29G=	XP_005250875.1:n.-29G=
XM_006716518.2:c.-29G=	XP_006716581.1:n.-29G=
XM_011516903.1:c.-29G=	XP_011515205.1:n.-29G=
XM_011516904.1:c.-29G=	XP_011515206.1:n.-29G=
XR_928507.1:n.112+962C=
XM_005250818.3:c.-29G=	XP_005250875.1:n.-29G=
XM_006716518.3:c.-29G=	XP_006716581.1:n.-29G=
XM_011516903.3:c.-29G=	XP_011515205.1:n.-29G=
XM_017013167.2:c.-29G=	XP_016868656.1:n.-29G=
XM_024447087.1:c.-29G=	XP_024302855.1:n.-29G=
XR_001745489.1:n.126G=
XR_001745490.2:n.126G=
XR_928507.2:n.233+962C=
NM_001385.3:c.-29G= MANE Select	NP_001376.1:n.-29G=