Canonical Allele Identifier: CA1730877632
Community Standard Title: NM_005045.4(RELN):c.578-3T=
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103749507A= , CM000669.2:g.103749507A= GRCh38
NC_000007.13:g.103389954A= , CM000669.1:g.103389954A= GRCh37
NC_000007.12:g.103177190A= NCBI36
NG_011877.1:g.245010T=
NG_011877.2:g.245010T=

Transcript Alleles

HGVS Amino-acid Change
NM_005045.4:c.578-3T= MANE Select NP_005036.2:n.578-3T=
ENST00000428762.6:c.578-3T= MANE Select ENSP00000392423.1:n.578-3T=
NM_005045.3:c.578-3T= NP_005036.2:n.578-3T=
NM_173054.2:c.578-3T= NP_774959.1:n.578-3T=
NM_173054.3:c.578-3T= NP_774959.1:n.578-3T=
ENST00000343529.9:c.578-3T= ENSP00000345694.5:n.578-3T=
ENST00000424685.2:c.578-3T= ENSP00000388446.2:n.578-3T=
ENST00000424685.3:c.578-3T= ENSP00000388446.3:n.578-3T=
ENST00000428762.5:c.578-3T= ENSP00000392423.1:n.578-3T=
ENST00000473457.2:n.842-3T=
ENST00000679867.1:n.462-3T=
ENST00000680712.1:n.392-3T=
ENST00000681034.1:c.578-3T= ENSP00000506075.1:n.578-3T=
ENST00000681401.1:n.854-3T=
ENST00000681931.1:n.462-3T=