Canonical Allele Identifier: CA368767663
Gene: RELN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103523391A>T , CM000669.2:g.103523391A>T GRCh38
NC_000007.13:g.103163838A>T , CM000669.1:g.103163838A>T GRCh37
NC_000007.12:g.102951074A>T NCBI36
NG_011877.1:g.471126T>A
NG_011877.2:g.471126T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.7490T>A ENSP00000388446.3:p.Val2497Asp
ENST00000428762.6:c.7490T>A MANE Select ENSP00000392423.1:p.Val2497Asp
ENST00000478148.2:n.731T>A
ENST00000679867.1:n.7374T>A
ENST00000679952.1:n.1418T>A
ENST00000681034.1:c.7490T>A ENSP00000506075.1:p.Val2497Asp
ENST00000681364.1:n.739T>A
ENST00000343529.9:c.7490T>A ENSP00000345694.5:p.Val2497Asp
ENST00000424685.2:c.7490T>A ENSP00000388446.2:p.Val2497Asp
ENST00000428762.5:c.7490T>A ENSP00000392423.1:p.Val2497Asp
NM_005045.3:c.7490T>A NP_005036.2:p.Val2497Asp
NM_173054.2:c.7490T>A NP_774959.1:p.Val2497Asp
NM_005045.4:c.7490T>A MANE Select NP_005036.2:p.Val2497Asp
NM_173054.3:c.7490T>A NP_774959.1:p.Val2497Asp