Canonical Allele Identifier: CA830820061

Gene: RELN

Linked Data

• dbSNP Id: rs3914132
• MyVariant Identifiers: chr7:g.103527369C>A (hg19) ; chr7:g.103886922C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103886922C>A , CM000669.2:g.103886922C>A	GRCh38
NC_000007.13:g.103527369C>A , CM000669.1:g.103527369C>A	GRCh37
NC_000007.12:g.103314605C>A	NCBI36
NG_011877.1:g.107595G>T
NG_011877.2:g.107595G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.337+30153G>T	ENSP00000388446.3:n.337+30153G>T
ENST00000428762.6:c.337+30153G>T MANE Select	ENSP00000392423.1:n.337+30153G>T
ENST00000473457.2:n.601+30153G>T
ENST00000679867.1:n.221+30153G>T
ENST00000680712.1:n.151+30153G>T
ENST00000681034.1:c.337+30153G>T	ENSP00000506075.1:n.337+30153G>T
ENST00000681401.1:n.613+30153G>T
ENST00000681931.1:n.221+30153G>T
ENST00000343529.9:c.337+30153G>T	ENSP00000345694.5:n.337+30153G>T
ENST00000424685.2:c.337+30153G>T	ENSP00000388446.2:n.337+30153G>T
ENST00000428762.5:c.337+30153G>T	ENSP00000392423.1:n.337+30153G>T
NM_005045.3:c.337+30153G>T	NP_005036.2:n.337+30153G>T
NM_173054.2:c.337+30153G>T	NP_774959.1:n.337+30153G>T
NM_005045.4:c.337+30153G>T MANE Select	NP_005036.2:n.337+30153G>T
NM_173054.3:c.337+30153G>T	NP_774959.1:n.337+30153G>T