Canonical Allele Identifier: CA368768005

Gene: RELN

Linked Data

• MyVariant Identifiers: chr7:g.103163965G>C (hg19) ; chr7:g.103523518G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523518G>C , CM000669.2:g.103523518G>C	GRCh38
NC_000007.13:g.103163965G>C , CM000669.1:g.103163965G>C	GRCh37
NC_000007.12:g.102951201G>C	NCBI36
NG_011877.1:g.470999C>G
NG_011877.2:g.470999C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7363C>G	ENSP00000388446.3:p.Arg2455Gly
ENST00000428762.6:c.7363C>G MANE Select	ENSP00000392423.1:p.Arg2455Gly
ENST00000478148.2:n.604C>G
ENST00000679867.1:n.7247C>G
ENST00000679952.1:n.1291C>G
ENST00000681034.1:c.7363C>G	ENSP00000506075.1:p.Arg2455Gly
ENST00000681364.1:n.612C>G
ENST00000343529.9:c.7363C>G	ENSP00000345694.5:p.Arg2455Gly
ENST00000424685.2:c.7363C>G	ENSP00000388446.2:p.Arg2455Gly
ENST00000428762.5:c.7363C>G	ENSP00000392423.1:p.Arg2455Gly
ENST00000478148.1:n.594C>G
NM_005045.3:c.7363C>G	NP_005036.2:p.Arg2455Gly
NM_173054.2:c.7363C>G	NP_774959.1:p.Arg2455Gly
NM_005045.4:c.7363C>G MANE Select	NP_005036.2:p.Arg2455Gly
NM_173054.3:c.7363C>G	NP_774959.1:p.Arg2455Gly