Canonical Allele Identifier: CA2578980928

Gene: RELN

Linked Data

• gnomAD v4: 7-103572328-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103572328G>A , CM000669.2:g.103572328G>A	GRCh38
NC_000007.13:g.103212775G>A , CM000669.1:g.103212775G>A	GRCh37
NC_000007.12:g.103000011G>A	NCBI36
NG_011877.1:g.422189C>T
NG_011877.2:g.422189C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.4512-68C>T	ENSP00000388446.3:n.4512-68C>T
ENST00000428762.6:c.4512-68C>T MANE Select	ENSP00000392423.1:n.4512-68C>T
ENST00000679867.1:n.4396-68C>T
ENST00000680706.1:n.2215-68C>T
ENST00000681034.1:c.4512-68C>T	ENSP00000506075.1:n.4512-68C>T
ENST00000343529.9:c.4512-68C>T	ENSP00000345694.5:n.4512-68C>T
ENST00000424685.2:c.4512-68C>T	ENSP00000388446.2:n.4512-68C>T
ENST00000428762.5:c.4512-68C>T	ENSP00000392423.1:n.4512-68C>T
NM_005045.3:c.4512-68C>T	NP_005036.2:n.4512-68C>T
NM_173054.2:c.4512-68C>T	NP_774959.1:n.4512-68C>T
NM_005045.4:c.4512-68C>T MANE Select	NP_005036.2:n.4512-68C>T
NM_173054.3:c.4512-68C>T	NP_774959.1:n.4512-68C>T