Canonical Allele Identifier: CA1730991712

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103985410C= , CM000669.2:g.103985410C=	GRCh38
NC_000007.13:g.103625857C= , CM000669.1:g.103625857C=	GRCh37
NC_000007.12:g.103413093C=	NCBI36
NG_011877.1:g.9107G=
NG_011877.2:g.9107G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.226+3721G=	ENSP00000388446.3:n.226+3721G=
ENST00000428762.6:c.226+3721G= MANE Select	ENSP00000392423.1:n.226+3721G=
ENST00000473457.2:n.490+3721G=
ENST00000679689.1:n.386+3721G=
ENST00000679867.1:n.110+3721G=
ENST00000680712.1:n.40+3721G=
ENST00000681034.1:c.226+3721G=	ENSP00000506075.1:n.226+3721G=
ENST00000681182.1:n.477+3721G=
ENST00000681401.1:n.502+3721G=
ENST00000681931.1:n.110+3721G=
ENST00000343529.9:c.226+3721G=	ENSP00000345694.5:n.226+3721G=
ENST00000424685.2:c.226+3721G=	ENSP00000388446.2:n.226+3721G=
ENST00000428762.5:c.226+3721G=	ENSP00000392423.1:n.226+3721G=
NM_005045.3:c.226+3721G=	NP_005036.2:n.226+3721G=
NM_173054.2:c.226+3721G=	NP_774959.1:n.226+3721G=
NM_005045.4:c.226+3721G= MANE Select	NP_005036.2:n.226+3721G=
NM_173054.3:c.226+3721G=	NP_774959.1:n.226+3721G=