Canonical Allele Identifier: CA368767702

Gene: RELN

Linked Data

• MyVariant Identifiers: chr7:g.103163855G>C (hg19) ; chr7:g.103523408G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523408G>C , CM000669.2:g.103523408G>C	GRCh38
NC_000007.13:g.103163855G>C , CM000669.1:g.103163855G>C	GRCh37
NC_000007.12:g.102951091G>C	NCBI36
NG_011877.1:g.471109C>G
NG_011877.2:g.471109C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7473C>G	ENSP00000388446.3:p.Cys2491Trp
ENST00000428762.6:c.7473C>G MANE Select	ENSP00000392423.1:p.Cys2491Trp
ENST00000478148.2:n.714C>G
ENST00000679867.1:n.7357C>G
ENST00000679952.1:n.1401C>G
ENST00000681034.1:c.7473C>G	ENSP00000506075.1:p.Cys2491Trp
ENST00000681364.1:n.722C>G
ENST00000343529.9:c.7473C>G	ENSP00000345694.5:p.Cys2491Trp
ENST00000424685.2:c.7473C>G	ENSP00000388446.2:p.Cys2491Trp
ENST00000428762.5:c.7473C>G	ENSP00000392423.1:p.Cys2491Trp
NM_005045.3:c.7473C>G	NP_005036.2:p.Cys2491Trp
NM_173054.2:c.7473C>G	NP_774959.1:p.Cys2491Trp
NM_005045.4:c.7473C>G MANE Select	NP_005036.2:p.Cys2491Trp
NM_173054.3:c.7473C>G	NP_774959.1:p.Cys2491Trp