Canonical Allele Identifier: CA2578980914
Gene: RELN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103572283dup , CM000669.2:g.103572283dup GRCh38
NC_000007.13:g.103212730dup , CM000669.1:g.103212730dup GRCh37
NC_000007.12:g.102999966dup NCBI36
NG_011877.1:g.422236dup
NG_011877.2:g.422236dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.4512-21dup ENSP00000388446.3:n.4512-21dup
ENST00000428762.6:c.4512-21dup MANE Select ENSP00000392423.1:n.4512-21dup
ENST00000679867.1:n.4396-21dup
ENST00000680706.1:n.2215-21dup
ENST00000681034.1:c.4512-21dup ENSP00000506075.1:n.4512-21dup
ENST00000343529.9:c.4512-21dup ENSP00000345694.5:n.4512-21dup
ENST00000424685.2:c.4512-21dup ENSP00000388446.2:n.4512-21dup
ENST00000428762.5:c.4512-21dup ENSP00000392423.1:n.4512-21dup
NM_005045.3:c.4512-21dup NP_005036.2:n.4512-21dup
NM_173054.2:c.4512-21dup NP_774959.1:n.4512-21dup
NM_005045.4:c.4512-21dup MANE Select NP_005036.2:n.4512-21dup
NM_173054.3:c.4512-21dup NP_774959.1:n.4512-21dup