Canonical Allele Identifier: CA2777254719

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103678416_103678418del , CM000669.2:g.103678416_103678418del	GRCh38
NC_000007.13:g.103318863_103318865del , CM000669.1:g.103318863_103318865del	GRCh37
NC_000007.12:g.103106099_103106101del	NCBI36
NG_011877.1:g.316103_316105del
NG_011877.2:g.316103_316105del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.1289+3702_1289+3704del	ENSP00000388446.3:n.1289+3702_1289+3704del
ENST00000428762.6:c.1289+3702_1289+3704del MANE Select	ENSP00000392423.1:n.1289+3702_1289+3704del
ENST00000473457.2:n.1553+3702_1553+3704del
ENST00000679867.1:n.1173+3702_1173+3704del
ENST00000680712.1:n.1006+3702_1006+3704del
ENST00000681034.1:c.1289+3702_1289+3704del	ENSP00000506075.1:n.1289+3702_1289+3704del
ENST00000681931.1:n.1173+3702_1173+3704del
ENST00000343529.9:c.1289+3702_1289+3704del	ENSP00000345694.5:n.1289+3702_1289+3704del
ENST00000424685.2:c.1289+3702_1289+3704del	ENSP00000388446.2:n.1289+3702_1289+3704del
ENST00000428762.5:c.1289+3702_1289+3704del	ENSP00000392423.1:n.1289+3702_1289+3704del
NM_005045.3:c.1289+3702_1289+3704del	NP_005036.2:n.1289+3702_1289+3704del
NM_173054.2:c.1289+3702_1289+3704del	NP_774959.1:n.1289+3702_1289+3704del
NM_005045.4:c.1289+3702_1289+3704del MANE Select	NP_005036.2:n.1289+3702_1289+3704del
NM_173054.3:c.1289+3702_1289+3704del	NP_774959.1:n.1289+3702_1289+3704del