Canonical Allele Identifier: CA1807671399

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379456A= , CM000670.2:g.104379456A=	GRCh38
NC_000008.10:g.105391684A= , CM000670.1:g.105391684A=	GRCh37
NC_000008.9:g.105460860A=	NCBI36
NG_008840.1:g.92594T=
NG_008840.2:g.92594T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.*402T= MANE Select	ENSP00000276651.2:n.*402T=
ENST00000351513.6:c.*402T=	ENSP00000276651.2:n.*402T=
ENST00000520806.1:n.616T=
ENST00000521601.1:n.328+1728T=
NM_001385.2:c.*402T=	NP_001376.1:n.*402T=
XM_005250818.2:c.*402T=	XP_005250875.1:n.*402T=
XM_006716518.2:c.*402T=	XP_006716581.1:n.*402T=
XM_005250818.3:c.*402T=	XP_005250875.1:n.*402T=
XM_006716518.3:c.*402T=	XP_006716581.1:n.*402T=
XM_024447087.1:c.*939T=	XP_024302855.1:n.*939T=
XR_001745489.1:n.2561T=
XR_001745490.2:n.2453T=
NM_001385.3:c.*402T= MANE Select	NP_001376.1:n.*402T=