Canonical Allele Identifier: CA368767783
Gene: RELN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103523442C>A , CM000669.2:g.103523442C>A GRCh38
NC_000007.13:g.103163889C>A , CM000669.1:g.103163889C>A GRCh37
NC_000007.12:g.102951125C>A NCBI36
NG_011877.1:g.471075G>T
NG_011877.2:g.471075G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.7439G>T ENSP00000388446.3:p.Gly2480Val
ENST00000428762.6:c.7439G>T MANE Select ENSP00000392423.1:p.Gly2480Val
ENST00000478148.2:n.680G>T
ENST00000679867.1:n.7323G>T
ENST00000679952.1:n.1367G>T
ENST00000681034.1:c.7439G>T ENSP00000506075.1:p.Gly2480Val
ENST00000681364.1:n.688G>T
ENST00000343529.9:c.7439G>T ENSP00000345694.5:p.Gly2480Val
ENST00000424685.2:c.7439G>T ENSP00000388446.2:p.Gly2480Val
ENST00000428762.5:c.7439G>T ENSP00000392423.1:p.Gly2480Val
NM_005045.3:c.7439G>T NP_005036.2:p.Gly2480Val
NM_173054.2:c.7439G>T NP_774959.1:p.Gly2480Val
NM_005045.4:c.7439G>T MANE Select NP_005036.2:p.Gly2480Val
NM_173054.3:c.7439G>T NP_774959.1:p.Gly2480Val