Canonical Allele Identifier: CA368762876
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103515258A>C , CM000669.2:g.103515258A>C GRCh38
NC_000007.13:g.103155705A>C , CM000669.1:g.103155705A>C GRCh37
NC_000007.12:g.102942941A>C NCBI36
NG_011877.1:g.479259T>G
NG_011877.2:g.479259T>G

Transcript Alleles

HGVS Amino-acid Change
NM_005045.4:c.8046T>G MANE Select NP_005036.2:p.His2682Gln
ENST00000428762.6:c.8046T>G MANE Select ENSP00000392423.1:p.His2682Gln
NM_005045.3:c.8046T>G NP_005036.2:p.His2682Gln
NM_173054.2:c.8046T>G NP_774959.1:p.His2682Gln
NM_173054.3:c.8046T>G NP_774959.1:p.His2682Gln
ENST00000343529.9:c.8046T>G ENSP00000345694.5:p.His2682Gln
ENST00000424685.2:c.8046T>G ENSP00000388446.2:p.His2682Gln
ENST00000424685.3:c.8046T>G ENSP00000388446.3:p.His2682Gln
ENST00000428762.5:c.8046T>G ENSP00000392423.1:p.His2682Gln
ENST00000679867.1:n.7930T>G
ENST00000680248.1:n.1598T>G
ENST00000681034.1:c.8046T>G ENSP00000506075.1:p.His2682Gln
ENST00000681364.1:n.1295T>G