Canonical Allele Identifier: CA669986648

Gene: IDE

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92462867C>G , CM000672.2:g.92462867C>G	GRCh38
NC_000010.10:g.94222624C>G , CM000672.1:g.94222624C>G	GRCh37
NC_000010.9:g.94212604C>G	NCBI36
NG_013012.1:g.116229G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650060.2:c.2761+864G>C	ENSP00000497272.1:n.2761+864G>C
ENST00000265986.11:c.2761+864G>C MANE Select	ENSP00000265986.6:n.2761+864G>C
ENST00000650060.1:c.2761+864G>C	ENSP00000497272.1:n.2761+864G>C
ENST00000676540.1:c.2839+864G>C	ENSP00000504633.1:n.2839+864G>C
ENST00000676626.1:n.3647+864G>C
ENST00000676816.1:c.2762-263G>C	ENSP00000504709.1:n.2762-263G>C
ENST00000676987.1:n.2184-1615G>C
ENST00000677079.1:c.2761+864G>C	ENSP00000503417.1:n.2761+864G>C
ENST00000677096.1:c.*2757+864G>C	ENSP00000503793.1:n.*2757+864G>C
ENST00000677193.1:n.3721+864G>C
ENST00000677434.1:c.*1004+864G>C	ENSP00000503274.1:n.*1004+864G>C
ENST00000677569.1:c.*1458+864G>C	ENSP00000503462.1:n.*1458+864G>C
ENST00000678026.1:n.3647+864G>C
ENST00000678082.1:n.1326+864G>C
ENST00000678458.1:n.2753+864G>C
ENST00000678673.1:c.2321-1615G>C	ENSP00000503082.1:n.2321-1615G>C
ENST00000678715.1:c.2638+864G>C	ENSP00000503025.1:n.2638+864G>C
ENST00000678824.1:c.988+864G>C	ENSP00000503571.1:n.988+864G>C
ENST00000678844.1:c.*1055+864G>C	ENSP00000504561.1:n.*1055+864G>C
ENST00000678977.1:n.4336+864G>C
ENST00000679069.1:n.4333+864G>C
ENST00000679089.1:c.2489-1615G>C	ENSP00000504067.1:n.2489-1615G>C
ENST00000679174.1:c.*1514+864G>C	ENSP00000504758.1:n.*1514+864G>C
ENST00000679222.1:c.*1313+864G>C	ENSP00000504070.1:n.*1313+864G>C
ENST00000679232.1:c.*2808+864G>C	ENSP00000503818.1:n.*2808+864G>C
ENST00000679304.1:n.2435+864G>C
ENST00000679312.1:c.*867+864G>C	ENSP00000504442.1:n.*867+864G>C
ENST00000265986.10:c.2761+864G>C	ENSP00000265986.6:n.2761+864G>C
ENST00000371581.9:c.1096+864G>C	ENSP00000360637.5:n.1096+864G>C
ENST00000496903.5:n.1393+864G>C
NM_001165946.1:c.1096+864G>C	NP_001159418.1:n.1096+864G>C
NM_004969.3:c.2761+864G>C	NP_004960.2:n.2761+864G>C
XM_005269766.2:c.2761+864G>C	XP_005269823.1:n.2761+864G>C
NM_001322793.1:c.2761+864G>C	NP_001309722.1:n.2761+864G>C
NM_001322794.1:c.2644+864G>C	NP_001309723.1:n.2644+864G>C
NM_001322795.1:c.2638+864G>C	NP_001309724.1:n.2638+864G>C
NM_001322796.1:c.2638+864G>C	NP_001309725.1:n.2638+864G>C
NM_001322797.1:c.1096+864G>C	NP_001309726.1:n.1096+864G>C
NR_136399.1:n.2961+864G>C
XM_017016187.1:c.2638+864G>C	XP_016871676.1:n.2638+864G>C
XM_017016188.1:c.2638+864G>C	XP_016871677.1:n.2638+864G>C
XM_017016189.1:c.2638+864G>C	XP_016871678.1:n.2638+864G>C
XM_017016190.1:c.2638+864G>C	XP_016871679.1:n.2638+864G>C
NM_004969.4:c.2761+864G>C MANE Select	NP_004960.2:n.2761+864G>C
NM_001165946.2:c.1096+864G>C	NP_001159418.1:n.1096+864G>C
NM_001322793.2:c.2761+864G>C	NP_001309722.1:n.2761+864G>C
NM_001322794.2:c.2644+864G>C	NP_001309723.1:n.2644+864G>C
NM_001322795.2:c.2638+864G>C	NP_001309724.1:n.2638+864G>C
NM_001322797.2:c.1096+864G>C	NP_001309726.1:n.1096+864G>C
NR_136399.2:n.2959+864G>C