Canonical Allele Identifier: CA1730821973

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103635518G= , CM000669.2:g.103635518G=	GRCh38
NC_000007.13:g.103275965G= , CM000669.1:g.103275965G=	GRCh37
NC_000007.12:g.103063201G=	NCBI36
NG_011877.1:g.358999C=
NG_011877.2:g.358999C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.2372C=	ENSP00000388446.3:p.Pro791=
ENST00000428762.6:c.2372C= MANE Select	ENSP00000392423.1:p.Pro791=
ENST00000473457.2:n.2636C=
ENST00000679867.1:n.2256C=
ENST00000680706.1:n.75C=
ENST00000680712.1:n.2089C=
ENST00000681034.1:c.2372C=	ENSP00000506075.1:p.Pro791=
ENST00000343529.9:c.2372C=	ENSP00000345694.5:p.Pro791=
ENST00000424685.2:c.2372C=	ENSP00000388446.2:p.Pro791=
ENST00000428762.5:c.2372C=	ENSP00000392423.1:p.Pro791=
NM_005045.3:c.2372C=	NP_005036.2:p.Pro791=
NM_173054.2:c.2372C=	NP_774959.1:p.Pro791=
NM_005045.4:c.2372C= MANE Select	NP_005036.2:p.Pro791=
NM_173054.3:c.2372C=	NP_774959.1:p.Pro791=