Canonical Allele Identifier: CA1807671427

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379513_104379514delinsTA , CM000670.2:g.104379513_104379514delinsTA	GRCh38
NC_000008.10:g.105391741_105391742delinsTA , CM000670.1:g.105391741_105391742delinsTA	GRCh37
NC_000008.9:g.105460917_105460918delinsTA	NCBI36
NG_008840.1:g.92536_92537delinsTA
NG_008840.2:g.92536_92537delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.*344_*345delinsTA MANE Select	ENSP00000276651.2:n.*344_*345delinsTA
ENST00000351513.6:c.*344_*345delinsTA	ENSP00000276651.2:n.*344_*345delinsTA
ENST00000520806.1:n.558_559delinsTA
ENST00000521601.1:n.328+1670_328+1671delinsTA
ENST00000533874.1:c.403_404delinsTA
NM_001385.2:c.*344_*345delinsTA	NP_001376.1:n.*344_*345delinsTA
XM_005250818.2:c.*344_*345delinsTA	XP_005250875.1:n.*344_*345delinsTA
XM_006716518.2:c.*344_*345delinsTA	XP_006716581.1:n.*344_*345delinsTA
XM_005250818.3:c.*344_*345delinsTA	XP_005250875.1:n.*344_*345delinsTA
XM_006716518.3:c.*344_*345delinsTA	XP_006716581.1:n.*344_*345delinsTA
XM_024447087.1:c.*881_*882delinsTA	XP_024302855.1:n.*881_*882delinsTA
XR_001745489.1:n.2503_2504delinsTA
XR_001745490.2:n.2395_2396delinsTA
NM_001385.3:c.*344_*345delinsTA MANE Select	NP_001376.1:n.*344_*345delinsTA