Canonical Allele Identifier: CA2684377728

Gene: RELN

Linked Data

• gnomAD v4: 7-103572280-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103572283del , CM000669.2:g.103572283del	GRCh38
NC_000007.13:g.103212730del , CM000669.1:g.103212730del	GRCh37
NC_000007.12:g.102999966del	NCBI36
NG_011877.1:g.422236del
NG_011877.2:g.422236del

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.4512-21del	ENSP00000388446.3:n.4512-21del
ENST00000428762.6:c.4512-21del MANE Select	ENSP00000392423.1:n.4512-21del
ENST00000679867.1:n.4396-21del
ENST00000680706.1:n.2215-21del
ENST00000681034.1:c.4512-21del	ENSP00000506075.1:n.4512-21del
ENST00000343529.9:c.4512-21del	ENSP00000345694.5:n.4512-21del
ENST00000424685.2:c.4512-21del	ENSP00000388446.2:n.4512-21del
ENST00000428762.5:c.4512-21del	ENSP00000392423.1:n.4512-21del
NM_005045.3:c.4512-21del	NP_005036.2:n.4512-21del
NM_173054.2:c.4512-21del	NP_774959.1:n.4512-21del
NM_005045.4:c.4512-21del MANE Select	NP_005036.2:n.4512-21del
NM_173054.3:c.4512-21del	NP_774959.1:n.4512-21del