Canonical Allele Identifier: CA13164603

Gene: IDE

Linked Data

• dbSNP Id: rs7899603
• gnomAD v2: 10-94225017-G-C
• gnomAD v3: 10-92465260-G-C
• gnomAD v4: 10-92465260-G-C
• MyVariant Identifiers: chr10:g.94225017G>C (hg19) ; chr10:g.92465260G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92465260G>C , CM000672.2:g.92465260G>C	GRCh38
NC_000010.10:g.94225017G>C , CM000672.1:g.94225017G>C	GRCh37
NC_000010.9:g.94214997G>C	NCBI36
NG_013012.1:g.113836C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650060.2:c.2488+416C>G	ENSP00000497272.1:n.2488+416C>G
ENST00000265986.11:c.2488+416C>G MANE Select	ENSP00000265986.6:n.2488+416C>G
ENST00000650060.1:c.2488+416C>G	ENSP00000497272.1:n.2488+416C>G
ENST00000676540.1:c.2489-156C>G	ENSP00000504633.1:n.2489-156C>G
ENST00000676626.1:n.3374+416C>G
ENST00000676816.1:c.2488+416C>G	ENSP00000504709.1:n.2488+416C>G
ENST00000676987.1:n.2183+3619C>G
ENST00000677079.1:c.2488+416C>G	ENSP00000503417.1:n.2488+416C>G
ENST00000677096.1:c.*2484+416C>G	ENSP00000503793.1:n.*2484+416C>G
ENST00000677193.1:n.3448+416C>G
ENST00000677434.1:c.*731+416C>G	ENSP00000503274.1:n.*731+416C>G
ENST00000677569.1:c.*1185+416C>G	ENSP00000503462.1:n.*1185+416C>G
ENST00000678026.1:n.3374+416C>G
ENST00000678082.1:n.1053+416C>G
ENST00000678458.1:n.2480+416C>G
ENST00000678673.1:c.2320+3619C>G	ENSP00000503082.1:n.2320+3619C>G
ENST00000678715.1:c.2365+416C>G	ENSP00000503025.1:n.2365+416C>G
ENST00000678824.1:c.715+416C>G	ENSP00000503571.1:n.715+416C>G
ENST00000678844.1:c.*782+416C>G	ENSP00000504561.1:n.*782+416C>G
ENST00000678977.1:n.4063+416C>G
ENST00000679069.1:n.4060+416C>G
ENST00000679089.1:c.2488+416C>G	ENSP00000504067.1:n.2488+416C>G
ENST00000679174.1:c.*1241+416C>G	ENSP00000504758.1:n.*1241+416C>G
ENST00000679222.1:c.*1040+416C>G	ENSP00000504070.1:n.*1040+416C>G
ENST00000679232.1:c.*2535+416C>G	ENSP00000503818.1:n.*2535+416C>G
ENST00000679304.1:n.2162+416C>G
ENST00000679312.1:c.*594+416C>G	ENSP00000504442.1:n.*594+416C>G
ENST00000265986.10:c.2488+416C>G	ENSP00000265986.6:n.2488+416C>G
ENST00000371581.9:c.823+416C>G	ENSP00000360637.5:n.823+416C>G
ENST00000496903.5:n.1120+416C>G
NM_001165946.1:c.823+416C>G	NP_001159418.1:n.823+416C>G
NM_004969.3:c.2488+416C>G	NP_004960.2:n.2488+416C>G
XM_005269766.2:c.2488+416C>G	XP_005269823.1:n.2488+416C>G
NM_001322793.1:c.2488+416C>G	NP_001309722.1:n.2488+416C>G
NM_001322794.1:c.2371+416C>G	NP_001309723.1:n.2371+416C>G
NM_001322795.1:c.2365+416C>G	NP_001309724.1:n.2365+416C>G
NM_001322796.1:c.2365+416C>G	NP_001309725.1:n.2365+416C>G
NM_001322797.1:c.823+416C>G	NP_001309726.1:n.823+416C>G
NR_136399.1:n.2688+416C>G
XM_017016187.1:c.2365+416C>G	XP_016871676.1:n.2365+416C>G
XM_017016188.1:c.2365+416C>G	XP_016871677.1:n.2365+416C>G
XM_017016189.1:c.2365+416C>G	XP_016871678.1:n.2365+416C>G
XM_017016190.1:c.2365+416C>G	XP_016871679.1:n.2365+416C>G
NM_004969.4:c.2488+416C>G MANE Select	NP_004960.2:n.2488+416C>G
NM_001165946.2:c.823+416C>G	NP_001159418.1:n.823+416C>G
NM_001322793.2:c.2488+416C>G	NP_001309722.1:n.2488+416C>G
NM_001322794.2:c.2371+416C>G	NP_001309723.1:n.2371+416C>G
NM_001322795.2:c.2365+416C>G	NP_001309724.1:n.2365+416C>G
NM_001322797.2:c.823+416C>G	NP_001309726.1:n.823+416C>G
NR_136399.2:n.2686+416C>G