Canonical Allele Identifier: CA1730783571
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103545502A= , CM000669.2:g.103545502A= GRCh38
NC_000007.13:g.103185949A= , CM000669.1:g.103185949A= GRCh37
NC_000007.12:g.102973185A= NCBI36
NG_011877.1:g.449015T=
NG_011877.2:g.449015T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.6303-158T= ENSP00000388446.3:n.6303-158T=
ENST00000428762.6:c.6303-158T= MANE Select ENSP00000392423.1:n.6303-158T=
ENST00000679867.1:n.6187-158T=
ENST00000679952.1:n.95-158T=
ENST00000681034.1:c.6303-158T= ENSP00000506075.1:n.6303-158T=
ENST00000681199.1:n.2071-158T=
ENST00000343529.9:c.6303-158T= ENSP00000345694.5:n.6303-158T=
ENST00000424685.2:c.6303-158T= ENSP00000388446.2:n.6303-158T=
ENST00000428762.5:c.6303-158T= ENSP00000392423.1:n.6303-158T=
NM_005045.3:c.6303-158T= NP_005036.2:n.6303-158T=
NM_173054.2:c.6303-158T= NP_774959.1:n.6303-158T=
NM_005045.4:c.6303-158T= MANE Select NP_005036.2:n.6303-158T=
NM_173054.3:c.6303-158T= NP_774959.1:n.6303-158T=