Canonical Allele Identifier: CA4420957
Gene: RELN HGNC NCBI

Linked Data

ClinVar Variation Id: 285255
dbSNP Id: rs144387303

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103545189C>T , CM000669.2:g.103545189C>T GRCh38
NC_000007.13:g.103185636C>T , CM000669.1:g.103185636C>T GRCh37
NC_000007.12:g.102972872C>T NCBI36
NG_011877.1:g.449328G>A
NG_011877.2:g.449328G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.6458G>A ENSP00000388446.3:p.Gly2153Asp
ENST00000428762.6:c.6458G>A MANE Select ENSP00000392423.1:p.Gly2153Asp
ENST00000679867.1:n.6342G>A
ENST00000679952.1:n.250G>A
ENST00000681034.1:c.6458G>A ENSP00000506075.1:p.Gly2153Asp
ENST00000681199.1:n.2226G>A
ENST00000343529.9:c.6458G>A ENSP00000345694.5:p.Gly2153Asp
ENST00000424685.2:c.6458G>A ENSP00000388446.2:p.Gly2153Asp
ENST00000428762.5:c.6458G>A ENSP00000392423.1:p.Gly2153Asp
NM_005045.3:c.6458G>A NP_005036.2:p.Gly2153Asp
NM_173054.2:c.6458G>A NP_774959.1:p.Gly2153Asp
NM_005045.4:c.6458G>A MANE Select NP_005036.2:p.Gly2153Asp
NM_173054.3:c.6458G>A NP_774959.1:p.Gly2153Asp