Canonical Allele Identifier: CA368771212

Gene: RELN

Linked Data

• MyVariant Identifiers: chr7:g.103185744T>C (hg19) ; chr7:g.103545297T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103545297T>C , CM000669.2:g.103545297T>C	GRCh38
NC_000007.13:g.103185744T>C , CM000669.1:g.103185744T>C	GRCh37
NC_000007.12:g.102972980T>C	NCBI36
NG_011877.1:g.449220A>G
NG_011877.2:g.449220A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.6350A>G	ENSP00000388446.3:p.Gln2117Arg
ENST00000428762.6:c.6350A>G MANE Select	ENSP00000392423.1:p.Gln2117Arg
ENST00000679867.1:n.6234A>G
ENST00000679952.1:n.142A>G
ENST00000681034.1:c.6350A>G	ENSP00000506075.1:p.Gln2117Arg
ENST00000681199.1:n.2118A>G
ENST00000343529.9:c.6350A>G	ENSP00000345694.5:p.Gln2117Arg
ENST00000424685.2:c.6350A>G	ENSP00000388446.2:p.Gln2117Arg
ENST00000428762.5:c.6350A>G	ENSP00000392423.1:p.Gln2117Arg
NM_005045.3:c.6350A>G	NP_005036.2:p.Gln2117Arg
NM_173054.2:c.6350A>G	NP_774959.1:p.Gln2117Arg
NM_005045.4:c.6350A>G MANE Select	NP_005036.2:p.Gln2117Arg
NM_173054.3:c.6350A>G	NP_774959.1:p.Gln2117Arg