Canonical Allele Identifier: CA2777251774
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103523727del , CM000669.2:g.103523727del GRCh38
NC_000007.13:g.103164174del , CM000669.1:g.103164174del GRCh37
NC_000007.12:g.102951410del NCBI36
NG_011877.1:g.470791del
NG_011877.2:g.470791del

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.7350-195del ENSP00000388446.3:n.7350-195del
ENST00000428762.6:c.7350-195del MANE Select ENSP00000392423.1:n.7350-195del
ENST00000478148.2:n.591-195del
ENST00000679867.1:n.7234-195del
ENST00000679952.1:n.1278-195del
ENST00000681034.1:c.7350-195del ENSP00000506075.1:n.7350-195del
ENST00000681364.1:n.599-195del
ENST00000343529.9:c.7350-195del ENSP00000345694.5:n.7350-195del
ENST00000424685.2:c.7350-195del ENSP00000388446.2:n.7350-195del
ENST00000428762.5:c.7350-195del ENSP00000392423.1:n.7350-195del
ENST00000478148.1:n.581-195del
NM_005045.3:c.7350-195del NP_005036.2:n.7350-195del
NM_173054.2:c.7350-195del NP_774959.1:n.7350-195del
NM_005045.4:c.7350-195del MANE Select NP_005036.2:n.7350-195del
NM_173054.3:c.7350-195del NP_774959.1:n.7350-195del