Canonical Allele Identifier: CA368760443

Gene: RELN

Linked Data

• MyVariant Identifiers: chr7:g.103276023A>C (hg19) ; chr7:g.103635576A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103635576A>C , CM000669.2:g.103635576A>C	GRCh38
NC_000007.13:g.103276023A>C , CM000669.1:g.103276023A>C	GRCh37
NC_000007.12:g.103063259A>C	NCBI36
NG_011877.1:g.358941T>G
NG_011877.2:g.358941T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.2314T>G	ENSP00000388446.3:p.Phe772Val
ENST00000428762.6:c.2314T>G MANE Select	ENSP00000392423.1:p.Phe772Val
ENST00000473457.2:n.2578T>G
ENST00000679867.1:n.2198T>G
ENST00000680706.1:n.17T>G
ENST00000680712.1:n.2031T>G
ENST00000681034.1:c.2314T>G	ENSP00000506075.1:p.Phe772Val
ENST00000343529.9:c.2314T>G	ENSP00000345694.5:p.Phe772Val
ENST00000424685.2:c.2314T>G	ENSP00000388446.2:p.Phe772Val
ENST00000428762.5:c.2314T>G	ENSP00000392423.1:p.Phe772Val
NM_005045.3:c.2314T>G	NP_005036.2:p.Phe772Val
NM_173054.2:c.2314T>G	NP_774959.1:p.Phe772Val
NM_005045.4:c.2314T>G MANE Select	NP_005036.2:p.Phe772Val
NM_173054.3:c.2314T>G	NP_774959.1:p.Phe772Val