Canonical Allele Identifier: CA368744432

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103561859G>A , CM000669.2:g.103561859G>A	GRCh38
NC_000007.13:g.103202306G>A , CM000669.1:g.103202306G>A	GRCh37
NC_000007.12:g.102989542G>A	NCBI36
NG_011877.1:g.432658C>T
NG_011877.2:g.432658C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.5305C>T	ENSP00000388446.3:p.Pro1769Ser
ENST00000428762.6:c.5305C>T MANE Select	ENSP00000392423.1:p.Pro1769Ser
ENST00000679867.1:n.5189C>T
ENST00000680706.1:n.3008C>T
ENST00000681034.1:c.5305C>T	ENSP00000506075.1:p.Pro1769Ser
ENST00000343529.9:c.5305C>T	ENSP00000345694.5:p.Pro1769Ser
ENST00000424685.2:c.5305C>T	ENSP00000388446.2:p.Pro1769Ser
ENST00000428762.5:c.5305C>T	ENSP00000392423.1:p.Pro1769Ser
NM_005045.3:c.5305C>T	NP_005036.2:p.Pro1769Ser
NM_173054.2:c.5305C>T	NP_774959.1:p.Pro1769Ser
NM_005045.4:c.5305C>T MANE Select	NP_005036.2:p.Pro1769Ser
NM_173054.3:c.5305C>T	NP_774959.1:p.Pro1769Ser