Canonical Allele Identifier: CA2500423294

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103535071T>A , CM000669.2:g.103535071T>A	GRCh38
NC_000007.13:g.103175518T>A , CM000669.1:g.103175518T>A	GRCh37
NC_000007.12:g.102962754T>A	NCBI36
NG_011877.1:g.459446A>T
NG_011877.2:g.459446A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.7349+245A>T	ENSP00000388446.3:n.7349+245A>T
ENST00000428762.6:c.7349+245A>T MANE Select	ENSP00000392423.1:n.7349+245A>T
ENST00000478148.2:n.590+245A>T
ENST00000679867.1:n.7233+245A>T
ENST00000679952.1:n.1141+245A>T
ENST00000681034.1:c.7349+245A>T	ENSP00000506075.1:n.7349+245A>T
ENST00000681315.1:n.1474A>T
ENST00000681364.1:n.598+245A>T
ENST00000343529.9:c.7349+245A>T	ENSP00000345694.5:n.7349+245A>T
ENST00000424685.2:c.7349+245A>T	ENSP00000388446.2:n.7349+245A>T
ENST00000428762.5:c.7349+245A>T	ENSP00000392423.1:n.7349+245A>T
ENST00000478148.1:n.580+245A>T
NM_005045.3:c.7349+245A>T	NP_005036.2:n.7349+245A>T
NM_173054.2:c.7349+245A>T	NP_774959.1:n.7349+245A>T
XR_927832.1:n.41+441T>A
NM_005045.4:c.7349+245A>T MANE Select	NP_005036.2:n.7349+245A>T
NM_173054.3:c.7349+245A>T	NP_774959.1:n.7349+245A>T