Canonical Allele Identifier: CA2740097450

Gene: RELN SLC26A5-AS1

Linked Data

• ClinVar Variation Id: 2941832
• ClinVar RCV Id: RCV003802854

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103483638A>G , CM000669.2:g.103483638A>G	GRCh38
NC_000007.13:g.103124085A>G , CM000669.1:g.103124085A>G	GRCh37
NC_000007.12:g.102911321A>G	NCBI36
NG_011877.1:g.510879T>C
NG_011877.2:g.510879T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.10181+15T>C (RELN)	ENSP00000388446.3:n.10181+15T>C
ENST00000428762.6:c.10181+15T>C (RELN) MANE Select	ENSP00000392423.1:n.10181+15T>C
ENST00000429186.2:c.92+15T>C (RELN)	ENSP00000404818.2:n.92+15T>C
ENST00000679371.1:n.1938+15T>C (RELN)
ENST00000679867.1:n.10065+15T>C (RELN)
ENST00000680248.1:n.3733+15T>C (RELN)
ENST00000681034.1:c.10181+15T>C (RELN)	ENSP00000506075.1:n.10181+15T>C
ENST00000681364.1:n.3430+15T>C (RELN)
ENST00000681921.1:n.4405+15T>C (RELN)
ENST00000343529.9:c.10181+15T>C (RELN)	ENSP00000345694.5:n.10181+15T>C
ENST00000424685.2:c.10181+15T>C (RELN)	ENSP00000388446.2:n.10181+15T>C
ENST00000428762.5:c.10181+15T>C (RELN)	ENSP00000392423.1:n.10181+15T>C
ENST00000473945.1:n.259+15T>C (RELN)
NM_005045.3:c.10181+15T>C (RELN)	NP_005036.2:n.10181+15T>C
NM_173054.2:c.10181+15T>C (RELN)	NP_774959.1:n.10181+15T>C
NR_110141.1:n.1366-20766A>G (SLC26A5-AS1)
NM_005045.4:c.10181+15T>C (RELN) MANE Select	NP_005036.2:n.10181+15T>C
NM_173054.3:c.10181+15T>C (RELN)	NP_774959.1:n.10181+15T>C