Canonical Allele Identifier: CA830797088

Gene: RELN

Linked Data

• dbSNP Id: rs1328241435
• gnomAD v3: 7-103523677-ATTC-A
• gnomAD v4: 7-103523677-ATTC-A
• MyVariant Identifiers: chr7:g.103164125_103164127del (hg19) ; chr7:g.103523678_103523680del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523683_103523685del , CM000669.2:g.103523683_103523685del	GRCh38
NC_000007.13:g.103164130_103164132del , CM000669.1:g.103164130_103164132del	GRCh37
NC_000007.12:g.102951366_102951368del	NCBI36
NG_011877.1:g.470837_470839del
NG_011877.2:g.470837_470839del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7350-149_7350-147del	ENSP00000388446.3:n.7350-149_7350-147del
ENST00000428762.6:c.7350-149_7350-147del MANE Select	ENSP00000392423.1:n.7350-149_7350-147del
ENST00000478148.2:n.591-149_591-147del
ENST00000679867.1:n.7234-149_7234-147del
ENST00000679952.1:n.1278-149_1278-147del
ENST00000681034.1:c.7350-149_7350-147del	ENSP00000506075.1:n.7350-149_7350-147del
ENST00000681364.1:n.599-149_599-147del
ENST00000343529.9:c.7350-149_7350-147del	ENSP00000345694.5:n.7350-149_7350-147del
ENST00000424685.2:c.7350-149_7350-147del	ENSP00000388446.2:n.7350-149_7350-147del
ENST00000428762.5:c.7350-149_7350-147del	ENSP00000392423.1:n.7350-149_7350-147del
ENST00000478148.1:n.581-149_581-147del
NM_005045.3:c.7350-149_7350-147del	NP_005036.2:n.7350-149_7350-147del
NM_173054.2:c.7350-149_7350-147del	NP_774959.1:n.7350-149_7350-147del
NM_005045.4:c.7350-149_7350-147del MANE Select	NP_005036.2:n.7350-149_7350-147del
NM_173054.3:c.7350-149_7350-147del	NP_774959.1:n.7350-149_7350-147del