Canonical Allele Identifier: CA1928190484

Gene: IDE

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92472490T>A , CM000672.2:g.92472490T>A	GRCh38
NC_000010.10:g.94232247T>A , CM000672.1:g.94232247T>A	GRCh37
NC_000010.9:g.94222227T>A	NCBI36
NG_013012.1:g.106606A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650060.2:c.2117-2145A>T	ENSP00000497272.1:n.2117-2145A>T
ENST00000265986.11:c.2117-2145A>T MANE Select	ENSP00000265986.6:n.2117-2145A>T
ENST00000650060.1:c.2117-2145A>T	ENSP00000497272.1:n.2117-2145A>T
ENST00000676540.1:c.2117-2145A>T	ENSP00000504633.1:n.2117-2145A>T
ENST00000676626.1:n.3003-2145A>T
ENST00000676816.1:c.2117-2145A>T	ENSP00000504709.1:n.2117-2145A>T
ENST00000676987.1:n.717-2145A>T
ENST00000677079.1:c.2117-2145A>T	ENSP00000503417.1:n.2117-2145A>T
ENST00000677096.1:c.*2113-2145A>T	ENSP00000503793.1:n.*2113-2145A>T
ENST00000677193.1:n.1814-2145A>T
ENST00000677434.1:c.*360-2145A>T	ENSP00000503274.1:n.*360-2145A>T
ENST00000677569.1:c.*814-2145A>T	ENSP00000503462.1:n.*814-2145A>T
ENST00000678026.1:n.3003-2145A>T
ENST00000678082.1:n.436-2145A>T
ENST00000678248.1:n.2339-2145A>T
ENST00000678458.1:n.2109-2145A>T
ENST00000678673.1:c.2117-2145A>T	ENSP00000503082.1:n.2117-2145A>T
ENST00000678715.1:c.1994-2145A>T	ENSP00000503025.1:n.1994-2145A>T
ENST00000678824.1:c.344-2145A>T	ENSP00000503571.1:n.344-2145A>T
ENST00000678844.1:c.*411-2145A>T	ENSP00000504561.1:n.*411-2145A>T
ENST00000678977.1:n.3692-2145A>T
ENST00000679069.1:n.3689-2145A>T
ENST00000679089.1:c.2117-2145A>T	ENSP00000504067.1:n.2117-2145A>T
ENST00000679174.1:c.*870-2145A>T	ENSP00000504758.1:n.*870-2145A>T
ENST00000679222.1:c.*669-2145A>T	ENSP00000504070.1:n.*669-2145A>T
ENST00000679232.1:c.*2164-2145A>T	ENSP00000503818.1:n.*2164-2145A>T
ENST00000679304.1:n.1791-2145A>T
ENST00000679312.1:c.*223-2145A>T	ENSP00000504442.1:n.*223-2145A>T
ENST00000265986.10:c.2117-2145A>T	ENSP00000265986.6:n.2117-2145A>T
ENST00000371581.9:c.452-2145A>T	ENSP00000360637.5:n.452-2145A>T
ENST00000496903.5:n.749-2145A>T
NM_001165946.1:c.452-2145A>T	NP_001159418.1:n.452-2145A>T
NM_004969.3:c.2117-2145A>T	NP_004960.2:n.2117-2145A>T
XM_005269766.2:c.2117-2145A>T	XP_005269823.1:n.2117-2145A>T
XR_945727.1:n.2336-2145A>T
NM_001322793.1:c.2117-2145A>T	NP_001309722.1:n.2117-2145A>T
NM_001322794.1:c.2000-2145A>T	NP_001309723.1:n.2000-2145A>T
NM_001322795.1:c.1994-2145A>T	NP_001309724.1:n.1994-2145A>T
NM_001322796.1:c.1994-2145A>T	NP_001309725.1:n.1994-2145A>T
NM_001322797.1:c.452-2145A>T	NP_001309726.1:n.452-2145A>T
NR_136399.1:n.2317-2145A>T
XM_017016187.1:c.1994-2145A>T	XP_016871676.1:n.1994-2145A>T
XM_017016188.1:c.1994-2145A>T	XP_016871677.1:n.1994-2145A>T
XM_017016189.1:c.1994-2145A>T	XP_016871678.1:n.1994-2145A>T
XM_017016190.1:c.1994-2145A>T	XP_016871679.1:n.1994-2145A>T
XR_001747103.2:n.2460-2145A>T
XR_945727.3:n.2336-2145A>T
NM_004969.4:c.2117-2145A>T MANE Select	NP_004960.2:n.2117-2145A>T
NM_001165946.2:c.452-2145A>T	NP_001159418.1:n.452-2145A>T
NM_001322793.2:c.2117-2145A>T	NP_001309722.1:n.2117-2145A>T
NM_001322794.2:c.2000-2145A>T	NP_001309723.1:n.2000-2145A>T
NM_001322795.2:c.1994-2145A>T	NP_001309724.1:n.1994-2145A>T
NM_001322797.2:c.452-2145A>T	NP_001309726.1:n.452-2145A>T
NR_136399.2:n.2315-2145A>T