Canonical Allele Identifier: CA368767658

Gene: RELN

Linked Data

• MyVariant Identifiers: chr7:g.103163836A>G (hg19) ; chr7:g.103523389A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523389A>G , CM000669.2:g.103523389A>G	GRCh38
NC_000007.13:g.103163836A>G , CM000669.1:g.103163836A>G	GRCh37
NC_000007.12:g.102951072A>G	NCBI36
NG_011877.1:g.471128T>C
NG_011877.2:g.471128T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7490+2T>C	ENSP00000388446.3:n.7490+2T>C
ENST00000428762.6:c.7490+2T>C MANE Select	ENSP00000392423.1:n.7490+2T>C
ENST00000478148.2:n.733T>C
ENST00000679867.1:n.7374+2T>C
ENST00000679952.1:n.1418+2T>C
ENST00000681034.1:c.7490+2T>C	ENSP00000506075.1:n.7490+2T>C
ENST00000681364.1:n.739+2T>C
ENST00000343529.9:c.7490+2T>C	ENSP00000345694.5:n.7490+2T>C
ENST00000424685.2:c.7490+2T>C	ENSP00000388446.2:n.7490+2T>C
ENST00000428762.5:c.7490+2T>C	ENSP00000392423.1:n.7490+2T>C
NM_005045.3:c.7490+2T>C	NP_005036.2:n.7490+2T>C
NM_173054.2:c.7490+2T>C	NP_774959.1:n.7490+2T>C
NM_005045.4:c.7490+2T>C MANE Select	NP_005036.2:n.7490+2T>C
NM_173054.3:c.7490+2T>C	NP_774959.1:n.7490+2T>C