Canonical Allele Identifier: CA1928200282
Gene: IDE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92487528T= , CM000672.2:g.92487528T= GRCh38
NC_000010.10:g.94247285T= , CM000672.1:g.94247285T= GRCh37
NC_000010.9:g.94237265T= NCBI36
NG_013012.1:g.91568A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650060.2:c.1534-210A= ENSP00000497272.1:n.1534-210A=
ENST00000265986.11:c.1534-210A= MANE Select ENSP00000265986.6:n.1534-210A=
ENST00000650060.1:c.1534-210A= ENSP00000497272.1:n.1534-210A=
ENST00000676540.1:c.1534-210A= ENSP00000504633.1:n.1534-210A=
ENST00000676626.1:n.2151-210A=
ENST00000676816.1:c.1534-210A= ENSP00000504709.1:n.1534-210A=
ENST00000676987.1:n.362-210A=
ENST00000677079.1:c.1534-210A= ENSP00000503417.1:n.1534-210A=
ENST00000677096.1:c.*1530-210A= ENSP00000503793.1:n.*1530-210A=
ENST00000677193.1:n.1231-210A=
ENST00000677196.1:n.1611-210A=
ENST00000677434.1:c.1534-210A= ENSP00000503274.1:n.1534-210A=
ENST00000677569.1:c.*86-210A= ENSP00000503462.1:n.*86-210A=
ENST00000677953.1:n.2057-210A=
ENST00000677978.1:c.*86-210A= ENSP00000503310.1:n.*86-210A=
ENST00000678026.1:n.2151-210A=
ENST00000678248.1:n.1611-210A=
ENST00000678410.1:n.327-210A=
ENST00000678458.1:n.1526-210A=
ENST00000678673.1:c.1534-210A= ENSP00000503082.1:n.1534-210A=
ENST00000678715.1:c.1411-210A= ENSP00000503025.1:n.1411-210A=
ENST00000678824.1:c.-364-210A= ENSP00000503571.1:n.-364-210A=
ENST00000678844.1:c.1534-210A= ENSP00000504561.1:n.1534-210A=
ENST00000678977.1:n.3109-210A=
ENST00000679069.1:n.1611-210A=
ENST00000679089.1:c.1534-210A= ENSP00000504067.1:n.1534-210A=
ENST00000679174.1:c.*287-210A= ENSP00000504758.1:n.*287-210A=
ENST00000679222.1:c.*86-210A= ENSP00000504070.1:n.*86-210A=
ENST00000679232.1:c.*86-210A= ENSP00000503818.1:n.*86-210A=
ENST00000679304.1:n.1208-210A=
ENST00000679312.1:c.1534-210A= ENSP00000504442.1:n.1534-210A=
ENST00000265986.10:c.1534-210A= ENSP00000265986.6:n.1534-210A=
ENST00000371581.9:c.-132-210A= ENSP00000360637.5:n.-132-210A=
ENST00000478361.6:c.*1744-210A= ENSP00000473506.1:n.*1744-210A=
ENST00000492362.1:n.182-210A=
ENST00000496903.5:n.166-210A=
NM_001165946.1:c.-132-210A= NP_001159418.1:n.-132-210A=
NM_004969.3:c.1534-210A= NP_004960.2:n.1534-210A=
XM_005269766.2:c.1534-210A= XP_005269823.1:n.1534-210A=
XM_005269769.3:c.1534-210A= XP_005269826.1:n.1534-210A=
XR_945727.1:n.1608-210A=
NM_001322793.1:c.1534-210A= NP_001309722.1:n.1534-210A=
NM_001322794.1:c.1417-210A= NP_001309723.1:n.1417-210A=
NM_001322795.1:c.1411-210A= NP_001309724.1:n.1411-210A=
NM_001322796.1:c.1411-210A= NP_001309725.1:n.1411-210A=
NM_001322797.1:c.-132-210A= NP_001309726.1:n.-132-210A=
NR_136399.1:n.1610-210A=
XM_017016187.1:c.1411-210A= XP_016871676.1:n.1411-210A=
XM_017016188.1:c.1411-210A= XP_016871677.1:n.1411-210A=
XM_017016189.1:c.1411-210A= XP_016871678.1:n.1411-210A=
XM_017016190.1:c.1411-210A= XP_016871679.1:n.1411-210A=
XR_001747103.2:n.1608-210A=
XR_945727.3:n.1608-210A=
NM_004969.4:c.1534-210A= MANE Select NP_004960.2:n.1534-210A=
NM_001165946.2:c.-132-210A= NP_001159418.1:n.-132-210A=
NM_001322793.2:c.1534-210A= NP_001309722.1:n.1534-210A=
NM_001322794.2:c.1417-210A= NP_001309723.1:n.1417-210A=
NM_001322795.2:c.1411-210A= NP_001309724.1:n.1411-210A=
NM_001322797.2:c.-132-210A= NP_001309726.1:n.-132-210A=
NR_136399.2:n.1608-210A=