Canonical Allele Identifier: CA1730783189
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103545155T= , CM000669.2:g.103545155T= GRCh38
NC_000007.13:g.103185602T= , CM000669.1:g.103185602T= GRCh37
NC_000007.12:g.102972838T= NCBI36
NG_011877.1:g.449362A=
NG_011877.2:g.449362A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.6492A= ENSP00000388446.3:p.Lys2164=
ENST00000428762.6:c.6492A= MANE Select ENSP00000392423.1:p.Lys2164=
ENST00000679867.1:n.6376A=
ENST00000679952.1:n.284A=
ENST00000681034.1:c.6492A= ENSP00000506075.1:p.Lys2164=
ENST00000681199.1:n.2260A=
ENST00000343529.9:c.6492A= ENSP00000345694.5:p.Lys2164=
ENST00000424685.2:c.6492A= ENSP00000388446.2:p.Lys2164=
ENST00000428762.5:c.6492A= ENSP00000392423.1:p.Lys2164=
NM_005045.3:c.6492A= NP_005036.2:p.Lys2164=
NM_173054.2:c.6492A= NP_774959.1:p.Lys2164=
NM_005045.4:c.6492A= MANE Select NP_005036.2:p.Lys2164=
NM_173054.3:c.6492A= NP_774959.1:p.Lys2164=