Canonical Allele Identifier: CA2523744954
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103523359_103523360insAACTGTGAAGTTGATGGATACTGTATCTTCATTCTTGCTTAGAGA , CM000669.2:g.103523359_103523360insAACTGTGAAGTTGATGGATACTGTATCTTCATTCTTGCTTAGAGA GRCh38
NC_000007.13:g.103163806_103163807insAACTGTGAAGTTGATGGATACTGTATCTTCATTCTTGCTTAGAGA , CM000669.1:g.103163806_103163807insAACTGTGAAGTTGATGGATACTGTATCTTCATTCTTGCTTAGAGA GRCh37
NC_000007.12:g.102951042_102951043insAACTGTGAAGTTGATGGATACTGTATCTTCATTCTTGCTTAGAGA NCBI36
NG_011877.1:g.471157_471158insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT
NG_011877.2:g.471157_471158insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT ENSP00000388446.3:n.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATAC...
ENST00000428762.6:c.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT MANE Select ENSP00000392423.1:n.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATAC...
ENST00000478148.2:n.762_763insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT
ENST00000679867.1:n.7374+31_7374+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT
ENST00000679952.1:n.1418+31_1418+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT
ENST00000681034.1:c.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT ENSP00000506075.1:n.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATAC...
ENST00000681364.1:n.739+31_739+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT
ENST00000343529.9:c.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT ENSP00000345694.5:n.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATAC...
ENST00000424685.2:c.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT ENSP00000388446.2:n.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATAC...
ENST00000428762.5:c.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT ENSP00000392423.1:n.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATAC...
NM_005045.3:c.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT NP_005036.2:n.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATC...
NM_173054.2:c.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT NP_774959.1:n.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATC...
NM_005045.4:c.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT MANE Select NP_005036.2:n.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATC...
NM_173054.3:c.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATCCATCAACTTCACAGTT NP_774959.1:n.7490+31_7490+32insTCTCTAAGCAAGAATGAAGATACAGTATC...