Canonical Allele Identifier: CA163852535

Gene: RELN

Linked Data

• dbSNP Id: rs993914684
• MyVariant Identifiers: chr7:g.103318970T>C (hg19) ; chr7:g.103678523T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103678523T>C , CM000669.2:g.103678523T>C	GRCh38
NC_000007.13:g.103318970T>C , CM000669.1:g.103318970T>C	GRCh37
NC_000007.12:g.103106206T>C	NCBI36
NG_011877.1:g.315994A>G
NG_011877.2:g.315994A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.1289+3593A>G	ENSP00000388446.3:n.1289+3593A>G
ENST00000428762.6:c.1289+3593A>G MANE Select	ENSP00000392423.1:n.1289+3593A>G
ENST00000473457.2:n.1553+3593A>G
ENST00000679867.1:n.1173+3593A>G
ENST00000680712.1:n.1006+3593A>G
ENST00000681034.1:c.1289+3593A>G	ENSP00000506075.1:n.1289+3593A>G
ENST00000681931.1:n.1173+3593A>G
ENST00000343529.9:c.1289+3593A>G	ENSP00000345694.5:n.1289+3593A>G
ENST00000424685.2:c.1289+3593A>G	ENSP00000388446.2:n.1289+3593A>G
ENST00000428762.5:c.1289+3593A>G	ENSP00000392423.1:n.1289+3593A>G
NM_005045.3:c.1289+3593A>G	NP_005036.2:n.1289+3593A>G
NM_173054.2:c.1289+3593A>G	NP_774959.1:n.1289+3593A>G
NM_005045.4:c.1289+3593A>G MANE Select	NP_005036.2:n.1289+3593A>G
NM_173054.3:c.1289+3593A>G	NP_774959.1:n.1289+3593A>G