Canonical Allele Identifier: CA1730926139

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103849282G= , CM000669.2:g.103849282G=	GRCh38
NC_000007.13:g.103489729G= , CM000669.1:g.103489729G=	GRCh37
NC_000007.12:g.103276965G=	NCBI36
NG_011877.1:g.145235C=
NG_011877.2:g.145235C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005045.4:c.338-15610C= MANE Select	NP_005036.2:n.338-15610C=
ENST00000428762.6:c.338-15610C= MANE Select	ENSP00000392423.1:n.338-15610C=
NM_005045.3:c.338-15610C=	NP_005036.2:n.338-15610C=
NM_173054.2:c.338-15610C=	NP_774959.1:n.338-15610C=
NM_173054.3:c.338-15610C=	NP_774959.1:n.338-15610C=
ENST00000343529.9:c.338-15610C=	ENSP00000345694.5:n.338-15610C=
ENST00000424685.2:c.338-15610C=	ENSP00000388446.2:n.338-15610C=
ENST00000424685.3:c.338-15610C=	ENSP00000388446.3:n.338-15610C=
ENST00000428762.5:c.338-15610C=	ENSP00000392423.1:n.338-15610C=
ENST00000473457.2:n.602-15610C=
ENST00000679867.1:n.222-15610C=
ENST00000680712.1:n.152-15610C=
ENST00000681034.1:c.338-15610C=	ENSP00000506075.1:n.338-15610C=
ENST00000681401.1:n.614-15610C=
ENST00000681931.1:n.222-15610C=