Canonical Allele Identifier: CA1730773582

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523768C= , CM000669.2:g.103523768C=	GRCh38
NC_000007.13:g.103164215C= , CM000669.1:g.103164215C=	GRCh37
NC_000007.12:g.102951451C=	NCBI36
NG_011877.1:g.470749G=
NG_011877.2:g.470749G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7350-237G=	ENSP00000388446.3:n.7350-237G=
ENST00000428762.6:c.7350-237G= MANE Select	ENSP00000392423.1:n.7350-237G=
ENST00000478148.2:n.591-237G=
ENST00000679867.1:n.7234-237G=
ENST00000679952.1:n.1278-237G=
ENST00000681034.1:c.7350-237G=	ENSP00000506075.1:n.7350-237G=
ENST00000681364.1:n.599-237G=
ENST00000343529.9:c.7350-237G=	ENSP00000345694.5:n.7350-237G=
ENST00000424685.2:c.7350-237G=	ENSP00000388446.2:n.7350-237G=
ENST00000428762.5:c.7350-237G=	ENSP00000392423.1:n.7350-237G=
ENST00000478148.1:n.581-237G=
NM_005045.3:c.7350-237G=	NP_005036.2:n.7350-237G=
NM_173054.2:c.7350-237G=	NP_774959.1:n.7350-237G=
NM_005045.4:c.7350-237G= MANE Select	NP_005036.2:n.7350-237G=
NM_173054.3:c.7350-237G=	NP_774959.1:n.7350-237G=