Canonical Allele Identifier: CA1730991703

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103985390A= , CM000669.2:g.103985390A=	GRCh38
NC_000007.13:g.103625837A= , CM000669.1:g.103625837A=	GRCh37
NC_000007.12:g.103413073A=	NCBI36
NG_011877.1:g.9127T=
NG_011877.2:g.9127T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.226+3741T=	ENSP00000388446.3:n.226+3741T=
ENST00000428762.6:c.226+3741T= MANE Select	ENSP00000392423.1:n.226+3741T=
ENST00000473457.2:n.490+3741T=
ENST00000679689.1:n.386+3741T=
ENST00000679867.1:n.110+3741T=
ENST00000680712.1:n.40+3741T=
ENST00000681034.1:c.226+3741T=	ENSP00000506075.1:n.226+3741T=
ENST00000681182.1:n.477+3741T=
ENST00000681401.1:n.502+3741T=
ENST00000681931.1:n.110+3741T=
ENST00000343529.9:c.226+3741T=	ENSP00000345694.5:n.226+3741T=
ENST00000424685.2:c.226+3741T=	ENSP00000388446.2:n.226+3741T=
ENST00000428762.5:c.226+3741T=	ENSP00000392423.1:n.226+3741T=
NM_005045.3:c.226+3741T=	NP_005036.2:n.226+3741T=
NM_173054.2:c.226+3741T=	NP_774959.1:n.226+3741T=
NM_005045.4:c.226+3741T= MANE Select	NP_005036.2:n.226+3741T=
NM_173054.3:c.226+3741T=	NP_774959.1:n.226+3741T=