Canonical Allele Identifier: CA457030493

Gene: RELN

Linked Data

• MyVariant Identifiers: chr7:g.103163858T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523411T>C , CM000669.2:g.103523411T>C	GRCh38
NC_000007.13:g.103163858T>C , CM000669.1:g.103163858T>C	GRCh37
NC_000007.12:g.102951094T>C	NCBI36
NG_011877.1:g.471106A>G
NG_011877.2:g.471106A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7470A>G	ENSP00000388446.3:p.Arg2490=
ENST00000428762.6:c.7470A>G MANE Select	ENSP00000392423.1:p.Arg2490=
ENST00000478148.2:n.711A>G
ENST00000679867.1:n.7354A>G
ENST00000679952.1:n.1398A>G
ENST00000681034.1:c.7470A>G	ENSP00000506075.1:p.Arg2490=
ENST00000681364.1:n.719A>G
ENST00000343529.9:c.7470A>G	ENSP00000345694.5:p.Arg2490=
ENST00000424685.2:c.7470A>G	ENSP00000388446.2:p.Arg2490=
ENST00000428762.5:c.7470A>G	ENSP00000392423.1:p.Arg2490=
NM_005045.3:c.7470A>G	NP_005036.2:p.Arg2490=
NM_173054.2:c.7470A>G	NP_774959.1:p.Arg2490=
NM_005045.4:c.7470A>G MANE Select	NP_005036.2:p.Arg2490=
NM_173054.3:c.7470A>G	NP_774959.1:p.Arg2490=