Canonical Allele Identifier: CA457026467

Gene: RELN

Linked Data

• dbSNP Id: rs1832560211
• MyVariant Identifiers: chr7:g.103275964A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103635517A>T , CM000669.2:g.103635517A>T	GRCh38
NC_000007.13:g.103275964A>T , CM000669.1:g.103275964A>T	GRCh37
NC_000007.12:g.103063200A>T	NCBI36
NG_011877.1:g.359000T>A
NG_011877.2:g.359000T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.2373T>A	ENSP00000388446.3:p.Pro791=
ENST00000428762.6:c.2373T>A MANE Select	ENSP00000392423.1:p.Pro791=
ENST00000473457.2:n.2637T>A
ENST00000679867.1:n.2257T>A
ENST00000680706.1:n.76T>A
ENST00000680712.1:n.2090T>A
ENST00000681034.1:c.2373T>A	ENSP00000506075.1:p.Pro791=
ENST00000343529.9:c.2373T>A	ENSP00000345694.5:p.Pro791=
ENST00000424685.2:c.2373T>A	ENSP00000388446.2:p.Pro791=
ENST00000428762.5:c.2373T>A	ENSP00000392423.1:p.Pro791=
NM_005045.3:c.2373T>A	NP_005036.2:p.Pro791=
NM_173054.2:c.2373T>A	NP_774959.1:p.Pro791=
NM_005045.4:c.2373T>A MANE Select	NP_005036.2:p.Pro791=
NM_173054.3:c.2373T>A	NP_774959.1:p.Pro791=