Canonical Allele Identifier: CA1730769713
Gene: RELN HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_005045.4:c.8046T= MANE Select NP_005036.2:p.His2682=
ENST00000428762.6:c.8046T= MANE Select ENSP00000392423.1:p.His2682=
NM_005045.3:c.8046T= NP_005036.2:p.His2682=
NM_173054.2:c.8046T= NP_774959.1:p.His2682=
NM_173054.3:c.8046T= NP_774959.1:p.His2682=
ENST00000343529.9:c.8046T= ENSP00000345694.5:p.His2682=
ENST00000424685.2:c.8046T= ENSP00000388446.2:p.His2682=
ENST00000424685.3:c.8046T= ENSP00000388446.3:p.His2682=
ENST00000428762.5:c.8046T= ENSP00000392423.1:p.His2682=
ENST00000679867.1:n.7930T=
ENST00000680248.1:n.1598T=
ENST00000681034.1:c.8046T= ENSP00000506075.1:p.His2682=
ENST00000681364.1:n.1295T=