Canonical Allele Identifier: CA1730758709

Gene: RELN SLC26A5-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103491969A= , CM000669.2:g.103491969A=	GRCh38
NC_000007.13:g.103132416A= , CM000669.1:g.103132416A=	GRCh37
NC_000007.12:g.102919652A=	NCBI36
NG_011877.1:g.502548T=
NG_011877.2:g.502548T=

Transcript Alleles

HGVS	Amino-acid Change
NM_005045.4:c.9427T= (RELN) MANE Select	NP_005036.2:p.Tyr3143=
ENST00000428762.6:c.9427T= (RELN) MANE Select	ENSP00000392423.1:p.Tyr3143=
NM_005045.3:c.9427T= (RELN)	NP_005036.2:p.Tyr3143=
NM_173054.2:c.9427T= (RELN)	NP_774959.1:p.Tyr3143=
NM_173054.3:c.9427T= (RELN)	NP_774959.1:p.Tyr3143=
NR_110141.1:n.1366-12435A= (SLC26A5-AS1)
ENST00000343529.9:c.9427T= (RELN)	ENSP00000345694.5:p.Tyr3143=
ENST00000424685.2:c.9427T= (RELN)	ENSP00000388446.2:p.Tyr3143=
ENST00000424685.3:c.9427T= (RELN)	ENSP00000388446.3:p.Tyr3143=
ENST00000428762.5:c.9427T= (RELN)	ENSP00000392423.1:p.Tyr3143=
ENST00000679371.1:n.1184T= (RELN)
ENST00000679867.1:n.9311T= (RELN)
ENST00000680248.1:n.2979T= (RELN)
ENST00000681034.1:c.9427T= (RELN)	ENSP00000506075.1:p.Tyr3143=
ENST00000681364.1:n.2676T= (RELN)
ENST00000681921.1:n.3651T= (RELN)