Canonical Allele Identifier: CA4420356

Gene: RELN SLC26A5-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103497946A>G , CM000669.2:g.103497946A>G	GRCh38
NC_000007.13:g.103138393A>G , CM000669.1:g.103138393A>G	GRCh37
NC_000007.12:g.102925629A>G	NCBI36
NG_011877.1:g.496571T>C
NG_011877.2:g.496571T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005045.4:c.8844-20T>C (RELN) MANE Select	NP_005036.2:n.8844-20T>C
ENST00000428762.6:c.8844-20T>C (RELN) MANE Select	ENSP00000392423.1:n.8844-20T>C
NM_005045.3:c.8844-20T>C (RELN)	NP_005036.2:n.8844-20T>C
NM_173054.2:c.8844-20T>C (RELN)	NP_774959.1:n.8844-20T>C
NM_173054.3:c.8844-20T>C (RELN)	NP_774959.1:n.8844-20T>C
NR_110141.1:n.1366-6458A>G (SLC26A5-AS1)
ENST00000343529.9:c.8844-20T>C (RELN)	ENSP00000345694.5:n.8844-20T>C
ENST00000424685.2:c.8844-20T>C (RELN)	ENSP00000388446.2:n.8844-20T>C
ENST00000424685.3:c.8844-20T>C (RELN)	ENSP00000388446.3:n.8844-20T>C
ENST00000428762.5:c.8844-20T>C (RELN)	ENSP00000392423.1:n.8844-20T>C
ENST00000679371.1:n.601-20T>C (RELN)
ENST00000679867.1:n.8728-20T>C (RELN)
ENST00000680248.1:n.2396-20T>C (RELN)
ENST00000681034.1:c.8844-20T>C (RELN)	ENSP00000506075.1:n.8844-20T>C
ENST00000681364.1:n.2093-20T>C (RELN)
ENST00000681921.1:n.3068-20T>C (RELN)