Canonical Allele Identifier: CA1730757606

Gene: RELN SLC26A5-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103489956A= , CM000669.2:g.103489956A=	GRCh38
NC_000007.13:g.103130403A= , CM000669.1:g.103130403A=	GRCh37
NC_000007.12:g.102917639A=	NCBI36
NG_011877.1:g.504561T=
NG_011877.2:g.504561T=

Transcript Alleles

HGVS	Amino-acid Change
NM_005045.4:c.9606-57T= (RELN) MANE Select	NP_005036.2:n.9606-57T=
ENST00000428762.6:c.9606-57T= (RELN) MANE Select	ENSP00000392423.1:n.9606-57T=
NM_005045.3:c.9606-57T= (RELN)	NP_005036.2:n.9606-57T=
NM_173054.2:c.9606-57T= (RELN)	NP_774959.1:n.9606-57T=
NM_173054.3:c.9606-57T= (RELN)	NP_774959.1:n.9606-57T=
NR_110141.1:n.1366-14448A= (SLC26A5-AS1)
ENST00000343529.9:c.9606-57T= (RELN)	ENSP00000345694.5:n.9606-57T=
ENST00000424685.2:c.9606-57T= (RELN)	ENSP00000388446.2:n.9606-57T=
ENST00000424685.3:c.9606-57T= (RELN)	ENSP00000388446.3:n.9606-57T=
ENST00000428762.5:c.9606-57T= (RELN)	ENSP00000392423.1:n.9606-57T=
ENST00000679371.1:n.1363-57T= (RELN)
ENST00000679867.1:n.9490-57T= (RELN)
ENST00000680248.1:n.3158-57T= (RELN)
ENST00000681034.1:c.9606-57T= (RELN)	ENSP00000506075.1:n.9606-57T=
ENST00000681364.1:n.2855-57T= (RELN)
ENST00000681921.1:n.3830-57T= (RELN)