Canonical Allele Identifier: CA1730783736
Gene: RELN HGNC NCBI

Linked Data

dbSNP Id: rs1830278839

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103545651_103545652insA , CM000669.2:g.103545651_103545652insA GRCh38
NC_000007.13:g.103186098_103186099insA , CM000669.1:g.103186098_103186099insA GRCh37
NC_000007.12:g.102973334_102973335insA NCBI36
NG_011877.1:g.448865_448866insT
NG_011877.2:g.448865_448866insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.6303-308_6303-307insT ENSP00000388446.3:n.6303-308_6303-307insT
ENST00000428762.6:c.6303-308_6303-307insT MANE Select ENSP00000392423.1:n.6303-308_6303-307insT
ENST00000679867.1:n.6187-308_6187-307insT
ENST00000679952.1:n.95-308_95-307insT
ENST00000681034.1:c.6303-308_6303-307insT ENSP00000506075.1:n.6303-308_6303-307insT
ENST00000681199.1:n.2071-308_2071-307insT
ENST00000343529.9:c.6303-308_6303-307insT ENSP00000345694.5:n.6303-308_6303-307insT
ENST00000424685.2:c.6303-308_6303-307insT ENSP00000388446.2:n.6303-308_6303-307insT
ENST00000428762.5:c.6303-308_6303-307insT ENSP00000392423.1:n.6303-308_6303-307insT
NM_005045.3:c.6303-308_6303-307insT NP_005036.2:n.6303-308_6303-307insT
NM_173054.2:c.6303-308_6303-307insT NP_774959.1:n.6303-308_6303-307insT
NM_005045.4:c.6303-308_6303-307insT MANE Select NP_005036.2:n.6303-308_6303-307insT
NM_173054.3:c.6303-308_6303-307insT NP_774959.1:n.6303-308_6303-307insT