Canonical Allele Identifier: CA368931541

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103989290C>T , CM000669.2:g.103989290C>T	GRCh38
NC_000007.13:g.103629737C>T , CM000669.1:g.103629737C>T	GRCh37
NC_000007.12:g.103416973C>T	NCBI36
NG_011877.1:g.5227G>A
NG_011877.2:g.5227G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.67G>A	ENSP00000388446.3:p.Ala23Thr
ENST00000428762.6:c.67G>A MANE Select	ENSP00000392423.1:p.Ala23Thr
ENST00000473457.2:n.331G>A
ENST00000679689.1:n.227G>A
ENST00000681034.1:c.67G>A	ENSP00000506075.1:p.Ala23Thr
ENST00000681182.1:n.318G>A
ENST00000681401.1:n.343G>A
ENST00000343529.9:c.67G>A	ENSP00000345694.5:p.Ala23Thr
ENST00000424685.2:c.67G>A	ENSP00000388446.2:p.Ala23Thr
ENST00000428762.5:c.67G>A	ENSP00000392423.1:p.Ala23Thr
NM_005045.3:c.67G>A	NP_005036.2:p.Ala23Thr
NM_173054.2:c.67G>A	NP_774959.1:p.Ala23Thr
NM_005045.4:c.67G>A MANE Select	NP_005036.2:p.Ala23Thr
NM_173054.3:c.67G>A	NP_774959.1:p.Ala23Thr