Canonical Allele Identifier: CA1730775519

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103534998G= , CM000669.2:g.103534998G=	GRCh38
NC_000007.13:g.103175445G= , CM000669.1:g.103175445G=	GRCh37
NC_000007.12:g.102962681G=	NCBI36
NG_011877.1:g.459519C=
NG_011877.2:g.459519C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.7349+318C=	ENSP00000388446.3:n.7349+318C=
ENST00000428762.6:c.7349+318C= MANE Select	ENSP00000392423.1:n.7349+318C=
ENST00000478148.2:n.590+318C=
ENST00000679867.1:n.7233+318C=
ENST00000679952.1:n.1141+318C=
ENST00000681034.1:c.7349+318C=	ENSP00000506075.1:n.7349+318C=
ENST00000681315.1:n.1547C=
ENST00000681364.1:n.598+318C=
ENST00000343529.9:c.7349+318C=	ENSP00000345694.5:n.7349+318C=
ENST00000424685.2:c.7349+318C=	ENSP00000388446.2:n.7349+318C=
ENST00000428762.5:c.7349+318C=	ENSP00000392423.1:n.7349+318C=
ENST00000478148.1:n.580+318C=
NM_005045.3:c.7349+318C=	NP_005036.2:n.7349+318C=
NM_173054.2:c.7349+318C=	NP_774959.1:n.7349+318C=
XR_927832.1:n.41+368G=
NM_005045.4:c.7349+318C= MANE Select	NP_005036.2:n.7349+318C=
NM_173054.3:c.7349+318C=	NP_774959.1:n.7349+318C=