Canonical Allele Identifier: CA2684358859

Gene: RELN

Linked Data

• gnomAD v4: 7-103523348-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523348G>A , CM000669.2:g.103523348G>A	GRCh38
NC_000007.13:g.103163795G>A , CM000669.1:g.103163795G>A	GRCh37
NC_000007.12:g.102951031G>A	NCBI36
NG_011877.1:g.471169C>T
NG_011877.2:g.471169C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7490+43C>T	ENSP00000388446.3:n.7490+43C>T
ENST00000428762.6:c.7490+43C>T MANE Select	ENSP00000392423.1:n.7490+43C>T
ENST00000478148.2:n.774C>T
ENST00000679867.1:n.7374+43C>T
ENST00000679952.1:n.1418+43C>T
ENST00000681034.1:c.7490+43C>T	ENSP00000506075.1:n.7490+43C>T
ENST00000681364.1:n.739+43C>T
ENST00000343529.9:c.7490+43C>T	ENSP00000345694.5:n.7490+43C>T
ENST00000424685.2:c.7490+43C>T	ENSP00000388446.2:n.7490+43C>T
ENST00000428762.5:c.7490+43C>T	ENSP00000392423.1:n.7490+43C>T
NM_005045.3:c.7490+43C>T	NP_005036.2:n.7490+43C>T
NM_173054.2:c.7490+43C>T	NP_774959.1:n.7490+43C>T
NM_005045.4:c.7490+43C>T MANE Select	NP_005036.2:n.7490+43C>T
NM_173054.3:c.7490+43C>T	NP_774959.1:n.7490+43C>T