Canonical Allele Identifier: CA4420462

Gene: RELN SLC26A5-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103500920G>A , CM000669.2:g.103500920G>A	GRCh38
NC_000007.13:g.103141367G>A , CM000669.1:g.103141367G>A	GRCh37
NC_000007.12:g.102928603G>A	NCBI36
NG_011877.1:g.493597C>T
NG_011877.2:g.493597C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.8492C>T (RELN)	ENSP00000388446.3:p.Pro2831Leu
ENST00000428762.6:c.8492C>T (RELN) MANE Select	ENSP00000392423.1:p.Pro2831Leu
ENST00000679371.1:n.249C>T (RELN)
ENST00000679867.1:n.8376C>T (RELN)
ENST00000680248.1:n.2044C>T (RELN)
ENST00000681034.1:c.8492C>T (RELN)	ENSP00000506075.1:p.Pro2831Leu
ENST00000681364.1:n.1741C>T (RELN)
ENST00000681921.1:n.2716C>T (RELN)
ENST00000343529.9:c.8492C>T (RELN)	ENSP00000345694.5:p.Pro2831Leu
ENST00000424685.2:c.8492C>T (RELN)	ENSP00000388446.2:p.Pro2831Leu
ENST00000428762.5:c.8492C>T (RELN)	ENSP00000392423.1:p.Pro2831Leu
NM_005045.3:c.8492C>T (RELN)	NP_005036.2:p.Pro2831Leu
NM_173054.2:c.8492C>T (RELN)	NP_774959.1:p.Pro2831Leu
NR_110141.1:n.1366-3484G>A (SLC26A5-AS1)
NM_005045.4:c.8492C>T (RELN) MANE Select	NP_005036.2:p.Pro2831Leu
NM_173054.3:c.8492C>T (RELN)	NP_774959.1:p.Pro2831Leu