Canonical Allele Identifier: CA1105331101

Gene: RELN

Linked Data

• dbSNP Id: rs1269095638
• gnomAD v3: 7-103572330-C-A
• gnomAD v4: 7-103572330-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103572330C>A , CM000669.2:g.103572330C>A	GRCh38
NC_000007.13:g.103212777C>A , CM000669.1:g.103212777C>A	GRCh37
NC_000007.12:g.103000013C>A	NCBI36
NG_011877.1:g.422187G>T
NG_011877.2:g.422187G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.4512-70G>T	ENSP00000388446.3:n.4512-70G>T
ENST00000428762.6:c.4512-70G>T MANE Select	ENSP00000392423.1:n.4512-70G>T
ENST00000679867.1:n.4396-70G>T
ENST00000680706.1:n.2215-70G>T
ENST00000681034.1:c.4512-70G>T	ENSP00000506075.1:n.4512-70G>T
ENST00000343529.9:c.4512-70G>T	ENSP00000345694.5:n.4512-70G>T
ENST00000424685.2:c.4512-70G>T	ENSP00000388446.2:n.4512-70G>T
ENST00000428762.5:c.4512-70G>T	ENSP00000392423.1:n.4512-70G>T
NM_005045.3:c.4512-70G>T	NP_005036.2:n.4512-70G>T
NM_173054.2:c.4512-70G>T	NP_774959.1:n.4512-70G>T
NM_005045.4:c.4512-70G>T MANE Select	NP_005036.2:n.4512-70G>T
NM_173054.3:c.4512-70G>T	NP_774959.1:n.4512-70G>T