Canonical Allele Identifier: CA1730886928

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103764271A= , CM000669.2:g.103764271A=	GRCh38
NC_000007.13:g.103404718A= , CM000669.1:g.103404718A=	GRCh37
NC_000007.12:g.103191954A=	NCBI36
NG_011877.1:g.230246T=
NG_011877.2:g.230246T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.545-11057T=	ENSP00000388446.3:n.545-11057T=
ENST00000428762.6:c.545-11057T= MANE Select	ENSP00000392423.1:n.545-11057T=
ENST00000473457.2:n.809-11057T=
ENST00000679867.1:n.429-11057T=
ENST00000680712.1:n.359-11057T=
ENST00000681034.1:c.545-11057T=	ENSP00000506075.1:n.545-11057T=
ENST00000681401.1:n.821-11057T=
ENST00000681931.1:n.429-11057T=
ENST00000343529.9:c.545-11057T=	ENSP00000345694.5:n.545-11057T=
ENST00000424685.2:c.545-11057T=	ENSP00000388446.2:n.545-11057T=
ENST00000428762.5:c.545-11057T=	ENSP00000392423.1:n.545-11057T=
NM_005045.3:c.545-11057T=	NP_005036.2:n.545-11057T=
NM_173054.2:c.545-11057T=	NP_774959.1:n.545-11057T=
NM_005045.4:c.545-11057T= MANE Select	NP_005036.2:n.545-11057T=
NM_173054.3:c.545-11057T=	NP_774959.1:n.545-11057T=