Canonical Allele Identifier: CA246332

Gene: RELN SLC26A5-AS1

Linked Data

• ClinVar Variation Id: 197937
• ClinVar RCV Id: RCV000179109 ; RCV001291198
• dbSNP Id: rs794727753
• MyVariant Identifiers: chr7:g.103143456_103143459del (hg19) ; chr7:g.103503009_103503012del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103503014_103503017del , CM000669.2:g.103503014_103503017del	GRCh38
NC_000007.13:g.103143461_103143464del , CM000669.1:g.103143461_103143464del	GRCh37
NC_000007.12:g.102930697_102930700del	NCBI36
NG_011877.1:g.491505_491508del
NG_011877.2:g.491505_491508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.8489+4_8489+7del (RELN)
ENST00000428762.6:c.8489+4_8489+7del (RELN)
ENST00000679867.1:n.8373+4_8373+7del (RELN)
ENST00000680248.1:n.2041+4_2041+7del (RELN)
ENST00000681034.1:c.8489+4_8489+7del (RELN)
ENST00000681364.1:n.1738+4_1738+7del (RELN)
ENST00000681921.1:n.624_627del (RELN)
ENST00000343529.9:c.8489+4_8489+7del (RELN)
ENST00000424685.2:c.8489+4_8489+7del (RELN)
ENST00000428762.5:c.8489+4_8489+7del (RELN)
NM_005045.3:c.8489+4_8489+7del (RELN)
NM_173054.2:c.8489+4_8489+7del (RELN)
NR_110141.1:n.1366-1390_1366-1387del (SLC26A5-AS1)
NM_005045.4:c.8489+4_8489+7del (RELN)
NM_173054.3:c.8489+4_8489+7del (RELN)