Canonical Allele Identifier: CA1807707885

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104466990G= , CM000670.2:g.104466990G=	GRCh38
NC_000008.10:g.105479218G= , CM000670.1:g.105479218G=	GRCh37
NC_000008.9:g.105548394G=	NCBI36
NG_008840.1:g.5060C=
NG_008840.2:g.5060C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.-70C= MANE Select	ENSP00000276651.2:n.-70C=
ENST00000351513.6:c.-70C=	ENSP00000276651.2:n.-70C=
ENST00000521573.2:c.-70C=	ENSP00000430246.2:n.-70C=
NM_001385.2:c.-70C=	NP_001376.1:n.-70C=
XM_005250818.2:c.-70C=	XP_005250875.1:n.-70C=
XM_006716518.2:c.-70C=	XP_006716581.1:n.-70C=
XM_011516903.1:c.-70C=	XP_011515205.1:n.-70C=
XM_011516904.1:c.-70C=	XP_011515206.1:n.-70C=
XR_928507.1:n.112+1003G=
XM_005250818.3:c.-70C=	XP_005250875.1:n.-70C=
XM_006716518.3:c.-70C=	XP_006716581.1:n.-70C=
XM_011516903.3:c.-70C=	XP_011515205.1:n.-70C=
XM_017013167.2:c.-70C=	XP_016868656.1:n.-70C=
XM_024447087.1:c.-70C=	XP_024302855.1:n.-70C=
XR_001745489.1:n.85C=
XR_001745490.2:n.85C=
XR_928507.2:n.233+1003G=
NM_001385.3:c.-70C= MANE Select	NP_001376.1:n.-70C=