Canonical Allele Identifier: CA457030516

Gene: RELN

Linked Data

• MyVariant Identifiers: chr7:g.103163903G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523456G>C , CM000669.2:g.103523456G>C	GRCh38
NC_000007.13:g.103163903G>C , CM000669.1:g.103163903G>C	GRCh37
NC_000007.12:g.102951139G>C	NCBI36
NG_011877.1:g.471061C>G
NG_011877.2:g.471061C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7425C>G	ENSP00000388446.3:p.Val2475=
ENST00000428762.6:c.7425C>G MANE Select	ENSP00000392423.1:p.Val2475=
ENST00000478148.2:n.666C>G
ENST00000679867.1:n.7309C>G
ENST00000679952.1:n.1353C>G
ENST00000681034.1:c.7425C>G	ENSP00000506075.1:p.Val2475=
ENST00000681364.1:n.674C>G
ENST00000343529.9:c.7425C>G	ENSP00000345694.5:p.Val2475=
ENST00000424685.2:c.7425C>G	ENSP00000388446.2:p.Val2475=
ENST00000428762.5:c.7425C>G	ENSP00000392423.1:p.Val2475=
NM_005045.3:c.7425C>G	NP_005036.2:p.Val2475=
NM_173054.2:c.7425C>G	NP_774959.1:p.Val2475=
NM_005045.4:c.7425C>G MANE Select	NP_005036.2:p.Val2475=
NM_173054.3:c.7425C>G	NP_774959.1:p.Val2475=