Canonical Allele Identifier: CA1105321176

Gene: RELN SLC26A5-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103478381G>T , CM000669.2:g.103478381G>T	GRCh38
NC_000007.13:g.103118828G>T , CM000669.1:g.103118828G>T	GRCh37
NC_000007.12:g.102906064G>T	NCBI36
NG_011877.1:g.516136C>A
NG_011877.2:g.516136C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.*6+8C>A (RELN)	ENSP00000388446.3:n.*6+8C>A
ENST00000428762.6:c.10286+8C>A (RELN) MANE Select	ENSP00000392423.1:n.10286+8C>A
ENST00000429186.2:c.192-4469C>A (RELN)	ENSP00000404818.2:n.192-4469C>A
ENST00000679371.1:n.2037+4492C>A (RELN)
ENST00000679867.1:n.14656C>A (RELN)
ENST00000680248.1:n.3832+4492C>A (RELN)
ENST00000681034.1:c.*89+8C>A (RELN)	ENSP00000506075.1:n.*89+8C>A
ENST00000681364.1:n.3529+4492C>A (RELN)
ENST00000343529.9:c.10280+4492C>A (RELN)	ENSP00000345694.5:n.10280+4492C>A
ENST00000424685.2:c.10280+4492C>A (RELN)	ENSP00000388446.2:n.10280+4492C>A
ENST00000428762.5:c.10286+8C>A (RELN)	ENSP00000392423.1:n.10286+8C>A
ENST00000429186.1:c.212+8C>A (RELN)
NM_005045.3:c.10286+8C>A (RELN)	NP_005036.2:n.10286+8C>A
NM_173054.2:c.10280+4492C>A (RELN)	NP_774959.1:n.10280+4492C>A
NR_110141.1:n.1366-26023G>T (SLC26A5-AS1)
NM_005045.4:c.10286+8C>A (RELN) MANE Select	NP_005036.2:n.10286+8C>A
NM_173054.3:c.10280+4492C>A (RELN)	NP_774959.1:n.10280+4492C>A