Canonical Allele Identifier: CA576939741

Gene: RELN

Linked Data

• dbSNP Id: rs1207835210
• gnomAD v2: 7-103186085-ATTTTG-A
• gnomAD v3: 7-103545638-ATTTTG-A
• gnomAD v4: 7-103545638-ATTTTG-A
• MyVariant Identifiers: chr7:g.103186086_103186090del (hg19) ; chr7:g.103545639_103545643del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103545643_103545647del , CM000669.2:g.103545643_103545647del	GRCh38
NC_000007.13:g.103186090_103186094del , CM000669.1:g.103186090_103186094del	GRCh37
NC_000007.12:g.102973326_102973330del	NCBI36
NG_011877.1:g.448874_448878del
NG_011877.2:g.448874_448878del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.6303-299_6303-295del	ENSP00000388446.3:n.6303-299_6303-295del
ENST00000428762.6:c.6303-299_6303-295del MANE Select	ENSP00000392423.1:n.6303-299_6303-295del
ENST00000679867.1:n.6187-299_6187-295del
ENST00000679952.1:n.95-299_95-295del
ENST00000681034.1:c.6303-299_6303-295del	ENSP00000506075.1:n.6303-299_6303-295del
ENST00000681199.1:n.2071-299_2071-295del
ENST00000343529.9:c.6303-299_6303-295del	ENSP00000345694.5:n.6303-299_6303-295del
ENST00000424685.2:c.6303-299_6303-295del	ENSP00000388446.2:n.6303-299_6303-295del
ENST00000428762.5:c.6303-299_6303-295del	ENSP00000392423.1:n.6303-299_6303-295del
NM_005045.3:c.6303-299_6303-295del	NP_005036.2:n.6303-299_6303-295del
NM_173054.2:c.6303-299_6303-295del	NP_774959.1:n.6303-299_6303-295del
NM_005045.4:c.6303-299_6303-295del MANE Select	NP_005036.2:n.6303-299_6303-295del
NM_173054.3:c.6303-299_6303-295del	NP_774959.1:n.6303-299_6303-295del