Canonical Allele Identifier: CA1730783397

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103545322G= , CM000669.2:g.103545322G=	GRCh38
NC_000007.13:g.103185769G= , CM000669.1:g.103185769G=	GRCh37
NC_000007.12:g.102973005G=	NCBI36
NG_011877.1:g.449195C=
NG_011877.2:g.449195C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.6325C=	ENSP00000388446.3:p.Gln2109=
ENST00000428762.6:c.6325C= MANE Select	ENSP00000392423.1:p.Gln2109=
ENST00000679867.1:n.6209C=
ENST00000679952.1:n.117C=
ENST00000681034.1:c.6325C=	ENSP00000506075.1:p.Gln2109=
ENST00000681199.1:n.2093C=
ENST00000343529.9:c.6325C=	ENSP00000345694.5:p.Gln2109=
ENST00000424685.2:c.6325C=	ENSP00000388446.2:p.Gln2109=
ENST00000428762.5:c.6325C=	ENSP00000392423.1:p.Gln2109=
NM_005045.3:c.6325C=	NP_005036.2:p.Gln2109=
NM_173054.2:c.6325C=	NP_774959.1:p.Gln2109=
NM_005045.4:c.6325C= MANE Select	NP_005036.2:p.Gln2109=
NM_173054.3:c.6325C=	NP_774959.1:p.Gln2109=