Canonical Allele Identifier: CA368771131

Gene: RELN

Linked Data

• ClinVar Variation Id: 1714631
• ClinVar RCV Id: RCV002299015
• MyVariant Identifiers: chr7:g.103185708C>T (hg19) ; chr7:g.103545261C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103545261C>T , CM000669.2:g.103545261C>T	GRCh38
NC_000007.13:g.103185708C>T , CM000669.1:g.103185708C>T	GRCh37
NC_000007.12:g.102972944C>T	NCBI36
NG_011877.1:g.449256G>A
NG_011877.2:g.449256G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.6386G>A	ENSP00000388446.3:p.Gly2129Asp
ENST00000428762.6:c.6386G>A MANE Select	ENSP00000392423.1:p.Gly2129Asp
ENST00000679867.1:n.6270G>A
ENST00000679952.1:n.178G>A
ENST00000681034.1:c.6386G>A	ENSP00000506075.1:p.Gly2129Asp
ENST00000681199.1:n.2154G>A
ENST00000343529.9:c.6386G>A	ENSP00000345694.5:p.Gly2129Asp
ENST00000424685.2:c.6386G>A	ENSP00000388446.2:p.Gly2129Asp
ENST00000428762.5:c.6386G>A	ENSP00000392423.1:p.Gly2129Asp
NM_005045.3:c.6386G>A	NP_005036.2:p.Gly2129Asp
NM_173054.2:c.6386G>A	NP_774959.1:p.Gly2129Asp
NM_005045.4:c.6386G>A MANE Select	NP_005036.2:p.Gly2129Asp
NM_173054.3:c.6386G>A	NP_774959.1:p.Gly2129Asp