Canonical Allele Identifier: CA2777251406

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103535010C>T , CM000669.2:g.103535010C>T	GRCh38
NC_000007.13:g.103175457C>T , CM000669.1:g.103175457C>T	GRCh37
NC_000007.12:g.102962693C>T	NCBI36
NG_011877.1:g.459507G>A
NG_011877.2:g.459507G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7349+306G>A	ENSP00000388446.3:n.7349+306G>A
ENST00000428762.6:c.7349+306G>A MANE Select	ENSP00000392423.1:n.7349+306G>A
ENST00000478148.2:n.590+306G>A
ENST00000679867.1:n.7233+306G>A
ENST00000679952.1:n.1141+306G>A
ENST00000681034.1:c.7349+306G>A	ENSP00000506075.1:n.7349+306G>A
ENST00000681315.1:n.1535G>A
ENST00000681364.1:n.598+306G>A
ENST00000343529.9:c.7349+306G>A	ENSP00000345694.5:n.7349+306G>A
ENST00000424685.2:c.7349+306G>A	ENSP00000388446.2:n.7349+306G>A
ENST00000428762.5:c.7349+306G>A	ENSP00000392423.1:n.7349+306G>A
ENST00000478148.1:n.580+306G>A
NM_005045.3:c.7349+306G>A	NP_005036.2:n.7349+306G>A
NM_173054.2:c.7349+306G>A	NP_774959.1:n.7349+306G>A
XR_927832.1:n.41+380C>T
NM_005045.4:c.7349+306G>A MANE Select	NP_005036.2:n.7349+306G>A
NM_173054.3:c.7349+306G>A	NP_774959.1:n.7349+306G>A