Canonical Allele Identifier: CA577197179

Gene: RELN

Linked Data

• dbSNP Id: rs1343600472
• gnomAD v2: 7-103276040-A-T
• gnomAD v4: 7-103635593-A-T
• MyVariant Identifiers: chr7:g.103276040A>T (hg19) ; chr7:g.103635593A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103635593A>T , CM000669.2:g.103635593A>T	GRCh38
NC_000007.13:g.103276040A>T , CM000669.1:g.103276040A>T	GRCh37
NC_000007.12:g.103063276A>T	NCBI36
NG_011877.1:g.358924T>A
NG_011877.2:g.358924T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.2304-7T>A	ENSP00000388446.3:n.2304-7T>A
ENST00000428762.6:c.2304-7T>A MANE Select	ENSP00000392423.1:n.2304-7T>A
ENST00000473457.2:n.2568-7T>A
ENST00000679867.1:n.2188-7T>A
ENST00000680712.1:n.2021-7T>A
ENST00000681034.1:c.2304-7T>A	ENSP00000506075.1:n.2304-7T>A
ENST00000343529.9:c.2304-7T>A	ENSP00000345694.5:n.2304-7T>A
ENST00000424685.2:c.2304-7T>A	ENSP00000388446.2:n.2304-7T>A
ENST00000428762.5:c.2304-7T>A	ENSP00000392423.1:n.2304-7T>A
NM_005045.3:c.2304-7T>A	NP_005036.2:n.2304-7T>A
NM_173054.2:c.2304-7T>A	NP_774959.1:n.2304-7T>A
NM_005045.4:c.2304-7T>A MANE Select	NP_005036.2:n.2304-7T>A
NM_173054.3:c.2304-7T>A	NP_774959.1:n.2304-7T>A