Canonical Allele Identifier: CA2523057716
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103572301C>A , CM000669.2:g.103572301C>A GRCh38
NC_000007.13:g.103212748C>A , CM000669.1:g.103212748C>A GRCh37
NC_000007.12:g.102999984C>A NCBI36
NG_011877.1:g.422216G>T
NG_011877.2:g.422216G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.4512-41G>T ENSP00000388446.3:n.4512-41G>T
ENST00000428762.6:c.4512-41G>T MANE Select ENSP00000392423.1:n.4512-41G>T
ENST00000679867.1:n.4396-41G>T
ENST00000680706.1:n.2215-41G>T
ENST00000681034.1:c.4512-41G>T ENSP00000506075.1:n.4512-41G>T
ENST00000343529.9:c.4512-41G>T ENSP00000345694.5:n.4512-41G>T
ENST00000424685.2:c.4512-41G>T ENSP00000388446.2:n.4512-41G>T
ENST00000428762.5:c.4512-41G>T ENSP00000392423.1:n.4512-41G>T
NM_005045.3:c.4512-41G>T NP_005036.2:n.4512-41G>T
NM_173054.2:c.4512-41G>T NP_774959.1:n.4512-41G>T
NM_005045.4:c.4512-41G>T MANE Select NP_005036.2:n.4512-41G>T
NM_173054.3:c.4512-41G>T NP_774959.1:n.4512-41G>T