Canonical Allele Identifier: CA577197094

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103594310T>C , CM000669.2:g.103594310T>C	GRCh38
NC_000007.13:g.103234757T>C , CM000669.1:g.103234757T>C	GRCh37
NC_000007.12:g.103021993T>C	NCBI36
NG_011877.1:g.400207A>G
NG_011877.2:g.400207A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.3711+11A>G	ENSP00000388446.3:n.3711+11A>G
ENST00000428762.6:c.3711+11A>G MANE Select	ENSP00000392423.1:n.3711+11A>G
ENST00000679867.1:n.3595+11A>G
ENST00000680706.1:n.1414+11A>G
ENST00000681034.1:c.3711+11A>G	ENSP00000506075.1:n.3711+11A>G
ENST00000343529.9:c.3711+11A>G	ENSP00000345694.5:n.3711+11A>G
ENST00000424685.2:c.3711+11A>G	ENSP00000388446.2:n.3711+11A>G
ENST00000428762.5:c.3711+11A>G	ENSP00000392423.1:n.3711+11A>G
NM_005045.3:c.3711+11A>G	NP_005036.2:n.3711+11A>G
NM_173054.2:c.3711+11A>G	NP_774959.1:n.3711+11A>G
NM_005045.4:c.3711+11A>G MANE Select	NP_005036.2:n.3711+11A>G
NM_173054.3:c.3711+11A>G	NP_774959.1:n.3711+11A>G