Canonical Allele Identifier: CA5603863

Gene: IDE

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92574070G>A , CM000672.2:g.92574070G>A	GRCh38
NC_000010.10:g.94333827G>A , CM000672.1:g.94333827G>A	GRCh37
NC_000010.9:g.94323807G>A	NCBI36
NG_013012.1:g.5026C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650060.2:c.-51C>T	ENSP00000497272.1:n.-51C>T
ENST00000265986.11:c.-51C>T MANE Select	ENSP00000265986.6:n.-51C>T
ENST00000650060.1:c.-51C>T	ENSP00000497272.1:n.-51C>T
ENST00000676540.1:c.-51C>T	ENSP00000504633.1:n.-51C>T
ENST00000677079.1:c.-51C>T	ENSP00000503417.1:n.-51C>T
ENST00000677196.1:n.27C>T
ENST00000677434.1:c.-51C>T	ENSP00000503274.1:n.-51C>T
ENST00000677569.1:c.-51C>T	ENSP00000503462.1:n.-51C>T
ENST00000677953.1:n.27C>T
ENST00000677978.1:c.-51C>T	ENSP00000503310.1:n.-51C>T
ENST00000678248.1:n.27C>T
ENST00000678673.1:c.-51C>T	ENSP00000503082.1:n.-51C>T
ENST00000678844.1:c.-51C>T	ENSP00000504561.1:n.-51C>T
ENST00000678977.1:n.27C>T
ENST00000679069.1:n.27C>T
ENST00000679089.1:c.-51C>T	ENSP00000504067.1:n.-51C>T
ENST00000679174.1:c.-51C>T	ENSP00000504758.1:n.-51C>T
ENST00000679222.1:c.-51C>T	ENSP00000504070.1:n.-51C>T
ENST00000679232.1:c.-51C>T	ENSP00000503818.1:n.-51C>T
ENST00000679312.1:c.-51C>T	ENSP00000504442.1:n.-51C>T
ENST00000265986.10:c.-51C>T	ENSP00000265986.6:n.-51C>T
NM_004969.3:c.-51C>T	NP_004960.2:n.-51C>T
XM_005269766.2:c.-51C>T	XP_005269823.1:n.-51C>T
XM_005269769.3:c.-51C>T	XP_005269826.1:n.-51C>T
XR_945727.1:n.24C>T
NM_001322793.1:c.-51C>T	NP_001309722.1:n.-51C>T
NM_001322794.1:c.-51C>T	NP_001309723.1:n.-51C>T
NM_001322795.1:c.-356C>T	NP_001309724.1:n.-356C>T
NR_136399.1:n.26C>T
XR_001747103.2:n.24C>T
XR_945727.3:n.24C>T
NM_004969.4:c.-51C>T MANE Select	NP_004960.2:n.-51C>T
NM_001322793.2:c.-51C>T	NP_001309722.1:n.-51C>T
NM_001322794.2:c.-51C>T	NP_001309723.1:n.-51C>T
NM_001322795.2:c.-356C>T	NP_001309724.1:n.-356C>T
NR_136399.2:n.24C>T