Canonical Allele Identifier: CA1807671410

Gene: DPYS

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.104379479_104379480delinsCA , CM000670.2:g.104379479_104379480delinsCA	GRCh38
NC_000008.10:g.105391707_105391708delinsCA , CM000670.1:g.105391707_105391708delinsCA	GRCh37
NC_000008.9:g.105460883_105460884delinsCA	NCBI36
NG_008840.1:g.92570_92571delinsTG
NG_008840.2:g.92570_92571delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351513.7:c.*378_*379delinsTG MANE Select	ENSP00000276651.2:n.*378_*379delinsTG
ENST00000351513.6:c.*378_*379delinsTG	ENSP00000276651.2:n.*378_*379delinsTG
ENST00000520806.1:n.592_593delinsTG
ENST00000521601.1:n.328+1704_328+1705delinsTG
NM_001385.2:c.*378_*379delinsTG	NP_001376.1:n.*378_*379delinsTG
XM_005250818.2:c.*378_*379delinsTG	XP_005250875.1:n.*378_*379delinsTG
XM_006716518.2:c.*378_*379delinsTG	XP_006716581.1:n.*378_*379delinsTG
XM_005250818.3:c.*378_*379delinsTG	XP_005250875.1:n.*378_*379delinsTG
XM_006716518.3:c.*378_*379delinsTG	XP_006716581.1:n.*378_*379delinsTG
XM_024447087.1:c.*915_*916delinsTG	XP_024302855.1:n.*915_*916delinsTG
XR_001745489.1:n.2537_2538delinsTG
XR_001745490.2:n.2429_2430delinsTG
NM_001385.3:c.*378_*379delinsTG MANE Select	NP_001376.1:n.*378_*379delinsTG