Canonical Allele Identifier: CA154904
Gene: RELN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103565283_103565296dup , CM000669.2:g.103565283_103565296dup GRCh38
NC_000007.13:g.103205730_103205743dup , CM000669.1:g.103205730_103205743dup GRCh37
NC_000007.12:g.102992966_102992979dup NCBI36
NG_011877.1:g.429224_429237dup
NG_011877.2:g.429224_429237dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.5195_5208dup ENSP00000388446.3:p.Ile1737PhefsTer?
ENST00000428762.6:c.5195_5208dup MANE Select ENSP00000392423.1:p.Ile1737PhefsTer?
ENST00000679867.1:n.5079_5092dup
ENST00000680706.1:n.2898_2911dup
ENST00000681034.1:c.5195_5208dup ENSP00000506075.1:p.Ile1737PhefsTer?
ENST00000343529.9:c.5195_5208dup ENSP00000345694.5:p.Ile1737PhefsTer?
ENST00000424685.2:c.5195_5208dup ENSP00000388446.2:p.Ile1737PhefsTer?
ENST00000428762.5:c.5195_5208dup ENSP00000392423.1:p.Ile1737PhefsTer?
NM_005045.3:c.5195_5208dup NP_005036.2:p.Ile1737PhefsTer?
NM_173054.2:c.5195_5208dup NP_774959.1:p.Ile1737PhefsTer?
NM_005045.4:c.5195_5208dup MANE Select NP_005036.2:p.Ile1737PhefsTer?
NM_173054.3:c.5195_5208dup NP_774959.1:p.Ile1737PhefsTer?
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