Canonical Allele Identifier: CA1730773414

Gene: RELN

Linked Data

• dbSNP Id: rs1829752202

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523359_103523371del , CM000669.2:g.103523359_103523371del	GRCh38
NC_000007.13:g.103163806_103163818del , CM000669.1:g.103163806_103163818del	GRCh37
NC_000007.12:g.102951042_102951054del	NCBI36
NG_011877.1:g.471146_471158del
NG_011877.2:g.471146_471158del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7490+20_7490+32del	ENSP00000388446.3:n.7490+20_7490+32del
ENST00000428762.6:c.7490+20_7490+32del MANE Select	ENSP00000392423.1:n.7490+20_7490+32del
ENST00000478148.2:n.751_763del
ENST00000679867.1:n.7374+20_7374+32del
ENST00000679952.1:n.1418+20_1418+32del
ENST00000681034.1:c.7490+20_7490+32del	ENSP00000506075.1:n.7490+20_7490+32del
ENST00000681364.1:n.739+20_739+32del
ENST00000343529.9:c.7490+20_7490+32del	ENSP00000345694.5:n.7490+20_7490+32del
ENST00000424685.2:c.7490+20_7490+32del	ENSP00000388446.2:n.7490+20_7490+32del
ENST00000428762.5:c.7490+20_7490+32del	ENSP00000392423.1:n.7490+20_7490+32del
NM_005045.3:c.7490+20_7490+32del	NP_005036.2:n.7490+20_7490+32del
NM_173054.2:c.7490+20_7490+32del	NP_774959.1:n.7490+20_7490+32del
NM_005045.4:c.7490+20_7490+32del MANE Select	NP_005036.2:n.7490+20_7490+32del
NM_173054.3:c.7490+20_7490+32del	NP_774959.1:n.7490+20_7490+32del