Canonical Allele Identifier: CA830797732

Gene: RELN

Linked Data

• dbSNP Id: rs39395
• MyVariant Identifiers: chr7:g.103489729G>C (hg19) ; chr7:g.103849282G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103849282G>C , CM000669.2:g.103849282G>C	GRCh38
NC_000007.13:g.103489729G>C , CM000669.1:g.103489729G>C	GRCh37
NC_000007.12:g.103276965G>C	NCBI36
NG_011877.1:g.145235C>G
NG_011877.2:g.145235C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.338-15610C>G	ENSP00000388446.3:n.338-15610C>G
ENST00000428762.6:c.338-15610C>G MANE Select	ENSP00000392423.1:n.338-15610C>G
ENST00000473457.2:n.602-15610C>G
ENST00000679867.1:n.222-15610C>G
ENST00000680712.1:n.152-15610C>G
ENST00000681034.1:c.338-15610C>G	ENSP00000506075.1:n.338-15610C>G
ENST00000681401.1:n.614-15610C>G
ENST00000681931.1:n.222-15610C>G
ENST00000343529.9:c.338-15610C>G	ENSP00000345694.5:n.338-15610C>G
ENST00000424685.2:c.338-15610C>G	ENSP00000388446.2:n.338-15610C>G
ENST00000428762.5:c.338-15610C>G	ENSP00000392423.1:n.338-15610C>G
NM_005045.3:c.338-15610C>G	NP_005036.2:n.338-15610C>G
NM_173054.2:c.338-15610C>G	NP_774959.1:n.338-15610C>G
NM_005045.4:c.338-15610C>G MANE Select	NP_005036.2:n.338-15610C>G
NM_173054.3:c.338-15610C>G	NP_774959.1:n.338-15610C>G