Canonical Allele Identifier: CA4420549

Gene: RELN SLC26A5-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103511020dup , CM000669.2:g.103511020dup	GRCh38
NC_000007.13:g.103151467dup , CM000669.1:g.103151467dup	GRCh37
NC_000007.12:g.102938703dup	NCBI36
NG_011877.1:g.483503dup
NG_011877.2:g.483503dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.8120-9dup (RELN)	ENSP00000388446.3:n.8120-9dup
ENST00000428762.6:c.8120-9dup (RELN) MANE Select	ENSP00000392423.1:n.8120-9dup
ENST00000679867.1:n.8004-9dup (RELN)
ENST00000680248.1:n.1672-9dup (RELN)
ENST00000681034.1:c.8120-9dup (RELN)	ENSP00000506075.1:n.8120-9dup
ENST00000681364.1:n.1369-9dup (RELN)
ENST00000681921.1:n.242dup (RELN)
ENST00000343529.9:c.8120-9dup (RELN)	ENSP00000345694.5:n.8120-9dup
ENST00000424685.2:c.8120-9dup (RELN)	ENSP00000388446.2:n.8120-9dup
ENST00000428762.5:c.8120-9dup (RELN)	ENSP00000392423.1:n.8120-9dup
NM_005045.3:c.8120-9dup (RELN)	NP_005036.2:n.8120-9dup
NM_173054.2:c.8120-9dup (RELN)	NP_774959.1:n.8120-9dup
NR_110141.1:n.1487-1749dup (SLC26A5-AS1)
NM_005045.4:c.8120-9dup (RELN) MANE Select	NP_005036.2:n.8120-9dup
NM_173054.3:c.8120-9dup (RELN)	NP_774959.1:n.8120-9dup