Canonical Allele Identifier: CA1730773450
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103523450G= , CM000669.2:g.103523450G= GRCh38
NC_000007.13:g.103163897G= , CM000669.1:g.103163897G= GRCh37
NC_000007.12:g.102951133G= NCBI36
NG_011877.1:g.471067C=
NG_011877.2:g.471067C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.7431C= ENSP00000388446.3:p.Ile2477=
ENST00000428762.6:c.7431C= MANE Select ENSP00000392423.1:p.Ile2477=
ENST00000478148.2:n.672C=
ENST00000679867.1:n.7315C=
ENST00000679952.1:n.1359C=
ENST00000681034.1:c.7431C= ENSP00000506075.1:p.Ile2477=
ENST00000681364.1:n.680C=
ENST00000343529.9:c.7431C= ENSP00000345694.5:p.Ile2477=
ENST00000424685.2:c.7431C= ENSP00000388446.2:p.Ile2477=
ENST00000428762.5:c.7431C= ENSP00000392423.1:p.Ile2477=
NM_005045.3:c.7431C= NP_005036.2:p.Ile2477=
NM_173054.2:c.7431C= NP_774959.1:p.Ile2477=
NM_005045.4:c.7431C= MANE Select NP_005036.2:p.Ile2477=
NM_173054.3:c.7431C= NP_774959.1:p.Ile2477=