Canonical Allele Identifier: CA1807671406

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379464T= , CM000670.2:g.104379464T=	GRCh38
NC_000008.10:g.105391692T= , CM000670.1:g.105391692T=	GRCh37
NC_000008.9:g.105460868T=	NCBI36
NG_008840.1:g.92586A=
NG_008840.2:g.92586A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.*394A= MANE Select	ENSP00000276651.2:n.*394A=
ENST00000351513.6:c.*394A=	ENSP00000276651.2:n.*394A=
ENST00000520806.1:n.608A=
ENST00000521601.1:n.328+1720A=
NM_001385.2:c.*394A=	NP_001376.1:n.*394A=
XM_005250818.2:c.*394A=	XP_005250875.1:n.*394A=
XM_006716518.2:c.*394A=	XP_006716581.1:n.*394A=
XM_005250818.3:c.*394A=	XP_005250875.1:n.*394A=
XM_006716518.3:c.*394A=	XP_006716581.1:n.*394A=
XM_024447087.1:c.*931A=	XP_024302855.1:n.*931A=
XR_001745489.1:n.2553A=
XR_001745490.2:n.2445A=
NM_001385.3:c.*394A= MANE Select	NP_001376.1:n.*394A=