Canonical Allele Identifier: CA4420306

Gene: RELN SLC26A5-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103496746A>G , CM000669.2:g.103496746A>G	GRCh38
NC_000007.13:g.103137193A>G , CM000669.1:g.103137193A>G	GRCh37
NC_000007.12:g.102924429A>G	NCBI36
NG_011877.1:g.497771T>C
NG_011877.2:g.497771T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.8973T>C (RELN)	ENSP00000388446.3:p.His2991=
ENST00000428762.6:c.8973T>C (RELN) MANE Select	ENSP00000392423.1:p.His2991=
ENST00000679371.1:n.730T>C (RELN)
ENST00000679867.1:n.8857T>C (RELN)
ENST00000680248.1:n.2525T>C (RELN)
ENST00000681034.1:c.8973T>C (RELN)	ENSP00000506075.1:p.His2991=
ENST00000681364.1:n.2222T>C (RELN)
ENST00000681921.1:n.3197T>C (RELN)
ENST00000343529.9:c.8973T>C (RELN)	ENSP00000345694.5:p.His2991=
ENST00000424685.2:c.8973T>C (RELN)	ENSP00000388446.2:p.His2991=
ENST00000428762.5:c.8973T>C (RELN)	ENSP00000392423.1:p.His2991=
NM_005045.3:c.8973T>C (RELN)	NP_005036.2:p.His2991=
NM_173054.2:c.8973T>C (RELN)	NP_774959.1:p.His2991=
NR_110141.1:n.1366-7658A>G (SLC26A5-AS1)
NM_005045.4:c.8973T>C (RELN) MANE Select	NP_005036.2:p.His2991=
NM_173054.3:c.8973T>C (RELN)	NP_774959.1:p.His2991=