Canonical Allele Identifier: CA368757793

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103629956G>A , CM000669.2:g.103629956G>A	GRCh38
NC_000007.13:g.103270403G>A , CM000669.1:g.103270403G>A	GRCh37
NC_000007.12:g.103057639G>A	NCBI36
NG_011877.1:g.364561C>T
NG_011877.2:g.364561C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.2686C>T	ENSP00000388446.3:p.His896Tyr
ENST00000428762.6:c.2686C>T MANE Select	ENSP00000392423.1:p.His896Tyr
ENST00000473457.2:n.2950C>T
ENST00000679867.1:n.2570C>T
ENST00000680706.1:n.389C>T
ENST00000681034.1:c.2686C>T	ENSP00000506075.1:p.His896Tyr
ENST00000343529.9:c.2686C>T	ENSP00000345694.5:p.His896Tyr
ENST00000424685.2:c.2686C>T	ENSP00000388446.2:p.His896Tyr
ENST00000428762.5:c.2686C>T	ENSP00000392423.1:p.His896Tyr
ENST00000473457.1:n.181C>T
NM_005045.3:c.2686C>T	NP_005036.2:p.His896Tyr
NM_173054.2:c.2686C>T	NP_774959.1:p.His896Tyr
NM_005045.4:c.2686C>T MANE Select	NP_005036.2:p.His896Tyr
NM_173054.3:c.2686C>T	NP_774959.1:p.His896Tyr