Canonical Allele Identifier: CA4422062

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103636414T>G , CM000669.2:g.103636414T>G	GRCh38
NC_000007.13:g.103276861T>G , CM000669.1:g.103276861T>G	GRCh37
NC_000007.12:g.103064097T>G	NCBI36
NG_011877.1:g.358103A>C
NG_011877.2:g.358103A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.2124A>C	ENSP00000388446.3:p.Pro708=
ENST00000428762.6:c.2124A>C MANE Select	ENSP00000392423.1:p.Pro708=
ENST00000473457.2:n.2388A>C
ENST00000679867.1:n.2008A>C
ENST00000680712.1:n.1841A>C
ENST00000681034.1:c.2124A>C	ENSP00000506075.1:p.Pro708=
ENST00000343529.9:c.2124A>C	ENSP00000345694.5:p.Pro708=
ENST00000424685.2:c.2124A>C	ENSP00000388446.2:p.Pro708=
ENST00000428762.5:c.2124A>C	ENSP00000392423.1:p.Pro708=
NM_005045.3:c.2124A>C	NP_005036.2:p.Pro708=
NM_173054.2:c.2124A>C	NP_774959.1:p.Pro708=
NM_005045.4:c.2124A>C MANE Select	NP_005036.2:p.Pro708=
NM_173054.3:c.2124A>C	NP_774959.1:p.Pro708=