Canonical Allele Identifier: CA1730886940
Gene: RELN HGNC NCBI

Linked Data

dbSNP Id: rs1791374673

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103764301T>C , CM000669.2:g.103764301T>C GRCh38
NC_000007.13:g.103404748T>C , CM000669.1:g.103404748T>C GRCh37
NC_000007.12:g.103191984T>C NCBI36
NG_011877.1:g.230216A>G
NG_011877.2:g.230216A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000424685.3:c.545-11087A>G ENSP00000388446.3:n.545-11087A>G
ENST00000428762.6:c.545-11087A>G MANE Select ENSP00000392423.1:n.545-11087A>G
ENST00000473457.2:n.809-11087A>G
ENST00000679867.1:n.429-11087A>G
ENST00000680712.1:n.359-11087A>G
ENST00000681034.1:c.545-11087A>G ENSP00000506075.1:n.545-11087A>G
ENST00000681401.1:n.821-11087A>G
ENST00000681931.1:n.429-11087A>G
ENST00000343529.9:c.545-11087A>G ENSP00000345694.5:n.545-11087A>G
ENST00000424685.2:c.545-11087A>G ENSP00000388446.2:n.545-11087A>G
ENST00000428762.5:c.545-11087A>G ENSP00000392423.1:n.545-11087A>G
NM_005045.3:c.545-11087A>G NP_005036.2:n.545-11087A>G
NM_173054.2:c.545-11087A>G NP_774959.1:n.545-11087A>G
NM_005045.4:c.545-11087A>G MANE Select NP_005036.2:n.545-11087A>G
NM_173054.3:c.545-11087A>G NP_774959.1:n.545-11087A>G