Canonical Allele Identifier: CA163918682

Gene: RELN

Linked Data

• dbSNP Id: rs932083509
• gnomAD v3: 7-103572337-GA-G
• gnomAD v4: 7-103572337-GA-G
• MyVariant Identifiers: chr7:g.103212785del (hg19) ; chr7:g.103572338del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103572344del , CM000669.2:g.103572344del	GRCh38
NC_000007.13:g.103212791del , CM000669.1:g.103212791del	GRCh37
NC_000007.12:g.103000027del	NCBI36
NG_011877.1:g.422179del
NG_011877.2:g.422179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.4512-78del	ENSP00000388446.3:n.4512-78del
ENST00000428762.6:c.4512-78del MANE Select	ENSP00000392423.1:n.4512-78del
ENST00000679867.1:n.4396-78del
ENST00000680706.1:n.2215-78del
ENST00000681034.1:c.4512-78del	ENSP00000506075.1:n.4512-78del
ENST00000343529.9:c.4512-78del	ENSP00000345694.5:n.4512-78del
ENST00000424685.2:c.4512-78del	ENSP00000388446.2:n.4512-78del
ENST00000428762.5:c.4512-78del	ENSP00000392423.1:n.4512-78del
NM_005045.3:c.4512-78del	NP_005036.2:n.4512-78del
NM_173054.2:c.4512-78del	NP_774959.1:n.4512-78del
NM_005045.4:c.4512-78del MANE Select	NP_005036.2:n.4512-78del
NM_173054.3:c.4512-78del	NP_774959.1:n.4512-78del