Canonical Allele Identifier: CA1730773448

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103523445_103523446delinsTC , CM000669.2:g.103523445_103523446delinsTC	GRCh38
NC_000007.13:g.103163892_103163893delinsTC , CM000669.1:g.103163892_103163893delinsTC	GRCh37
NC_000007.12:g.102951128_102951129delinsTC	NCBI36
NG_011877.1:g.471071_471072delinsGA
NG_011877.2:g.471071_471072delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7435_7436delinsGA	ENSP00000388446.3:p.Asp2479=
ENST00000428762.6:c.7435_7436delinsGA MANE Select	ENSP00000392423.1:p.Asp2479=
ENST00000478148.2:n.676_677delinsGA
ENST00000679867.1:n.7319_7320delinsGA
ENST00000679952.1:n.1363_1364delinsGA
ENST00000681034.1:c.7435_7436delinsGA	ENSP00000506075.1:p.Asp2479=
ENST00000681364.1:n.684_685delinsGA
ENST00000343529.9:c.7435_7436delinsGA	ENSP00000345694.5:p.Asp2479=
ENST00000424685.2:c.7435_7436delinsGA	ENSP00000388446.2:p.Asp2479=
ENST00000428762.5:c.7435_7436delinsGA	ENSP00000392423.1:p.Asp2479=
NM_005045.3:c.7435_7436delinsGA	NP_005036.2:p.Asp2479=
NM_173054.2:c.7435_7436delinsGA	NP_774959.1:p.Asp2479=
NM_005045.4:c.7435_7436delinsGA MANE Select	NP_005036.2:p.Asp2479=
NM_173054.3:c.7435_7436delinsGA	NP_774959.1:p.Asp2479=