Canonical Allele Identifier: CA1730773416
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103523365C= , CM000669.2:g.103523365C= GRCh38
NC_000007.13:g.103163812C= , CM000669.1:g.103163812C= GRCh37
NC_000007.12:g.102951048C= NCBI36
NG_011877.1:g.471152G=
NG_011877.2:g.471152G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.7490+26G= ENSP00000388446.3:n.7490+26G=
ENST00000428762.6:c.7490+26G= MANE Select ENSP00000392423.1:n.7490+26G=
ENST00000478148.2:n.757G=
ENST00000679867.1:n.7374+26G=
ENST00000679952.1:n.1418+26G=
ENST00000681034.1:c.7490+26G= ENSP00000506075.1:n.7490+26G=
ENST00000681364.1:n.739+26G=
ENST00000343529.9:c.7490+26G= ENSP00000345694.5:n.7490+26G=
ENST00000424685.2:c.7490+26G= ENSP00000388446.2:n.7490+26G=
ENST00000428762.5:c.7490+26G= ENSP00000392423.1:n.7490+26G=
NM_005045.3:c.7490+26G= NP_005036.2:n.7490+26G=
NM_173054.2:c.7490+26G= NP_774959.1:n.7490+26G=
NM_005045.4:c.7490+26G= MANE Select NP_005036.2:n.7490+26G=
NM_173054.3:c.7490+26G= NP_774959.1:n.7490+26G=