Canonical Allele Identifier: CA595249272

Gene: IDE

Linked Data

• dbSNP Id: rs11187007
• gnomAD v2: 10-94214580-A-C
• MyVariant Identifiers: chr10:g.94214580A>C (hg19) ; chr10:g.92454823A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92454823A>C , CM000672.2:g.92454823A>C	GRCh38
NC_000010.10:g.94214580A>C , CM000672.1:g.94214580A>C	GRCh37
NC_000010.9:g.94204560A>C	NCBI36
NG_013012.1:g.124273T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650060.2:c.2965-284T>G	ENSP00000497272.1:n.2965-284T>G
ENST00000265986.11:c.2965-284T>G MANE Select	ENSP00000265986.6:n.2965-284T>G
ENST00000650060.1:c.2965-284T>G	ENSP00000497272.1:n.2965-284T>G
ENST00000676540.1:c.2902-284T>G	ENSP00000504633.1:n.2902-284T>G
ENST00000676626.1:n.3710-284T>G
ENST00000676816.1:c.3086-284T>G	ENSP00000504709.1:n.3086-284T>G
ENST00000676987.1:n.2387-284T>G
ENST00000677079.1:c.2824-284T>G	ENSP00000503417.1:n.2824-284T>G
ENST00000677096.1:c.*2961-284T>G	ENSP00000503793.1:n.*2961-284T>G
ENST00000677193.1:n.3925-284T>G
ENST00000677434.1:c.*1960T>G	ENSP00000503274.1:n.*1960T>G
ENST00000677569.1:c.*1662-284T>G	ENSP00000503462.1:n.*1662-284T>G
ENST00000678026.1:n.3710-284T>G
ENST00000678082.1:n.1530-284T>G
ENST00000678097.1:n.1259-284T>G
ENST00000678458.1:n.2957-284T>G
ENST00000678673.1:c.2524-284T>G	ENSP00000503082.1:n.2524-284T>G
ENST00000678715.1:c.2842-284T>G	ENSP00000503025.1:n.2842-284T>G
ENST00000678824.1:c.1192-284T>G	ENSP00000503571.1:n.1192-284T>G
ENST00000678844.1:c.*1259-284T>G	ENSP00000504561.1:n.*1259-284T>G
ENST00000678977.1:n.4540-284T>G
ENST00000679069.1:n.4537-284T>G
ENST00000679089.1:c.2692-284T>G	ENSP00000504067.1:n.2692-284T>G
ENST00000679174.1:c.*1718-284T>G	ENSP00000504758.1:n.*1718-284T>G
ENST00000679222.1:c.*1517-284T>G	ENSP00000504070.1:n.*1517-284T>G
ENST00000679232.1:c.*3012-284T>G	ENSP00000503818.1:n.*3012-284T>G
ENST00000679304.1:n.2639-284T>G
ENST00000679312.1:c.*1071-284T>G	ENSP00000504442.1:n.*1071-284T>G
ENST00000265986.10:c.2965-284T>G	ENSP00000265986.6:n.2965-284T>G
ENST00000371581.9:c.1300-284T>G	ENSP00000360637.5:n.1300-284T>G
ENST00000496903.5:n.1597-284T>G
NM_001165946.1:c.1300-284T>G	NP_001159418.1:n.1300-284T>G
NM_004969.3:c.2965-284T>G	NP_004960.2:n.2965-284T>G
XM_005269766.2:c.2965-284T>G	XP_005269823.1:n.2965-284T>G
NM_001322793.1:c.2965-284T>G	NP_001309722.1:n.2965-284T>G
NM_001322794.1:c.2848-284T>G	NP_001309723.1:n.2848-284T>G
NM_001322795.1:c.2842-284T>G	NP_001309724.1:n.2842-284T>G
NM_001322796.1:c.2842-284T>G	NP_001309725.1:n.2842-284T>G
NM_001322797.1:c.1300-284T>G	NP_001309726.1:n.1300-284T>G
NR_136399.1:n.3165-284T>G
XM_017016187.1:c.2842-284T>G	XP_016871676.1:n.2842-284T>G
XM_017016188.1:c.2842-284T>G	XP_016871677.1:n.2842-284T>G
XM_017016189.1:c.2842-284T>G	XP_016871678.1:n.2842-284T>G
XM_017016190.1:c.2842-284T>G	XP_016871679.1:n.2842-284T>G
NM_004969.4:c.2965-284T>G MANE Select	NP_004960.2:n.2965-284T>G
NM_001165946.2:c.1300-284T>G	NP_001159418.1:n.1300-284T>G
NM_001322793.2:c.2965-284T>G	NP_001309722.1:n.2965-284T>G
NM_001322794.2:c.2848-284T>G	NP_001309723.1:n.2848-284T>G
NM_001322795.2:c.2842-284T>G	NP_001309724.1:n.2842-284T>G
NM_001322797.2:c.1300-284T>G	NP_001309726.1:n.1300-284T>G
NR_136399.2:n.3163-284T>G