Canonical Allele Identifier: CA164029022

Gene: RELN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103915467G>T , CM000669.2:g.103915467G>T	GRCh38
NC_000007.13:g.103555914G>T , CM000669.1:g.103555914G>T	GRCh37
NC_000007.12:g.103343150G>T	NCBI36
NG_011877.1:g.79050C>A
NG_011877.2:g.79050C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.337+1608C>A	ENSP00000388446.3:n.337+1608C>A
ENST00000428762.6:c.337+1608C>A MANE Select	ENSP00000392423.1:n.337+1608C>A
ENST00000473457.2:n.601+1608C>A
ENST00000679689.1:n.497+1608C>A
ENST00000679867.1:n.221+1608C>A
ENST00000680712.1:n.151+1608C>A
ENST00000681034.1:c.337+1608C>A	ENSP00000506075.1:n.337+1608C>A
ENST00000681182.1:n.2196C>A
ENST00000681401.1:n.613+1608C>A
ENST00000681931.1:n.221+1608C>A
ENST00000343529.9:c.337+1608C>A	ENSP00000345694.5:n.337+1608C>A
ENST00000424685.2:c.337+1608C>A	ENSP00000388446.2:n.337+1608C>A
ENST00000428762.5:c.337+1608C>A	ENSP00000392423.1:n.337+1608C>A
NM_005045.3:c.337+1608C>A	NP_005036.2:n.337+1608C>A
NM_173054.2:c.337+1608C>A	NP_774959.1:n.337+1608C>A
NM_005045.4:c.337+1608C>A MANE Select	NP_005036.2:n.337+1608C>A
NM_173054.3:c.337+1608C>A	NP_774959.1:n.337+1608C>A