Canonical Allele Identifier: CA368760155

Gene: RELN

Linked Data

• MyVariant Identifiers: chr7:g.103275971T>A (hg19) ; chr7:g.103635524T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103635524T>A , CM000669.2:g.103635524T>A	GRCh38
NC_000007.13:g.103275971T>A , CM000669.1:g.103275971T>A	GRCh37
NC_000007.12:g.103063207T>A	NCBI36
NG_011877.1:g.358993A>T
NG_011877.2:g.358993A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.2366A>T	ENSP00000388446.3:p.Asp789Val
ENST00000428762.6:c.2366A>T MANE Select	ENSP00000392423.1:p.Asp789Val
ENST00000473457.2:n.2630A>T
ENST00000679867.1:n.2250A>T
ENST00000680706.1:n.69A>T
ENST00000680712.1:n.2083A>T
ENST00000681034.1:c.2366A>T	ENSP00000506075.1:p.Asp789Val
ENST00000343529.9:c.2366A>T	ENSP00000345694.5:p.Asp789Val
ENST00000424685.2:c.2366A>T	ENSP00000388446.2:p.Asp789Val
ENST00000428762.5:c.2366A>T	ENSP00000392423.1:p.Asp789Val
NM_005045.3:c.2366A>T	NP_005036.2:p.Asp789Val
NM_173054.2:c.2366A>T	NP_774959.1:p.Asp789Val
NM_005045.4:c.2366A>T MANE Select	NP_005036.2:p.Asp789Val
NM_173054.3:c.2366A>T	NP_774959.1:p.Asp789Val