Canonical Allele Identifier: CA1730822083

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103635577C= , CM000669.2:g.103635577C=	GRCh38
NC_000007.13:g.103276024C= , CM000669.1:g.103276024C=	GRCh37
NC_000007.12:g.103063260C=	NCBI36
NG_011877.1:g.358940G=
NG_011877.2:g.358940G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.2313G=	ENSP00000388446.3:p.Gln771=
ENST00000428762.6:c.2313G= MANE Select	ENSP00000392423.1:p.Gln771=
ENST00000473457.2:n.2577G=
ENST00000679867.1:n.2197G=
ENST00000680706.1:n.16G=
ENST00000680712.1:n.2030G=
ENST00000681034.1:c.2313G=	ENSP00000506075.1:p.Gln771=
ENST00000343529.9:c.2313G=	ENSP00000345694.5:p.Gln771=
ENST00000424685.2:c.2313G=	ENSP00000388446.2:p.Gln771=
ENST00000428762.5:c.2313G=	ENSP00000392423.1:p.Gln771=
NM_005045.3:c.2313G=	NP_005036.2:p.Gln771=
NM_173054.2:c.2313G=	NP_774959.1:p.Gln771=
NM_005045.4:c.2313G= MANE Select	NP_005036.2:p.Gln771=
NM_173054.3:c.2313G=	NP_774959.1:p.Gln771=