Canonical Allele Identifier: CA2578980393

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523380_103523382del , CM000669.2:g.103523380_103523382del	GRCh38
NC_000007.13:g.103163827_103163829del , CM000669.1:g.103163827_103163829del	GRCh37
NC_000007.12:g.102951063_102951065del	NCBI36
NG_011877.1:g.471135_471137del
NG_011877.2:g.471135_471137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7490+9_7490+11del	ENSP00000388446.3:n.7490+9_7490+11del
ENST00000428762.6:c.7490+9_7490+11del MANE Select	ENSP00000392423.1:n.7490+9_7490+11del
ENST00000478148.2:n.740_742del
ENST00000679867.1:n.7374+9_7374+11del
ENST00000679952.1:n.1418+9_1418+11del
ENST00000681034.1:c.7490+9_7490+11del	ENSP00000506075.1:n.7490+9_7490+11del
ENST00000681364.1:n.739+9_739+11del
ENST00000343529.9:c.7490+9_7490+11del	ENSP00000345694.5:n.7490+9_7490+11del
ENST00000424685.2:c.7490+9_7490+11del	ENSP00000388446.2:n.7490+9_7490+11del
ENST00000428762.5:c.7490+9_7490+11del	ENSP00000392423.1:n.7490+9_7490+11del
NM_005045.3:c.7490+9_7490+11del	NP_005036.2:n.7490+9_7490+11del
NM_173054.2:c.7490+9_7490+11del	NP_774959.1:n.7490+9_7490+11del
NM_005045.4:c.7490+9_7490+11del MANE Select	NP_005036.2:n.7490+9_7490+11del
NM_173054.3:c.7490+9_7490+11del	NP_774959.1:n.7490+9_7490+11del