Canonical Allele Identifier: CA1807671425

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379507T= , CM000670.2:g.104379507T=	GRCh38
NC_000008.10:g.105391735T= , CM000670.1:g.105391735T=	GRCh37
NC_000008.9:g.105460911T=	NCBI36
NG_008840.1:g.92543A=
NG_008840.2:g.92543A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.*351A= MANE Select	ENSP00000276651.2:n.*351A=
ENST00000351513.6:c.*351A=	ENSP00000276651.2:n.*351A=
ENST00000520806.1:n.565A=
ENST00000521601.1:n.328+1677A=
ENST00000533874.1:c.410A=
NM_001385.2:c.*351A=	NP_001376.1:n.*351A=
XM_005250818.2:c.*351A=	XP_005250875.1:n.*351A=
XM_006716518.2:c.*351A=	XP_006716581.1:n.*351A=
XM_005250818.3:c.*351A=	XP_005250875.1:n.*351A=
XM_006716518.3:c.*351A=	XP_006716581.1:n.*351A=
XM_024447087.1:c.*888A=	XP_024302855.1:n.*888A=
XR_001745489.1:n.2510A=
XR_001745490.2:n.2402A=
NM_001385.3:c.*351A= MANE Select	NP_001376.1:n.*351A=