Canonical Allele Identifier: CA4420597

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103515334T>C , CM000669.2:g.103515334T>C	GRCh38
NC_000007.13:g.103155781T>C , CM000669.1:g.103155781T>C	GRCh37
NC_000007.12:g.102943017T>C	NCBI36
NG_011877.1:g.479183A>G
NG_011877.2:g.479183A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.7970A>G	ENSP00000388446.3:p.Asn2657Ser
ENST00000428762.6:c.7970A>G MANE Select	ENSP00000392423.1:p.Asn2657Ser
ENST00000679867.1:n.7854A>G
ENST00000680248.1:n.1522A>G
ENST00000681034.1:c.7970A>G	ENSP00000506075.1:p.Asn2657Ser
ENST00000681364.1:n.1219A>G
ENST00000343529.9:c.7970A>G	ENSP00000345694.5:p.Asn2657Ser
ENST00000424685.2:c.7970A>G	ENSP00000388446.2:p.Asn2657Ser
ENST00000428762.5:c.7970A>G	ENSP00000392423.1:p.Asn2657Ser
NM_005045.3:c.7970A>G	NP_005036.2:p.Asn2657Ser
NM_173054.2:c.7970A>G	NP_774959.1:p.Asn2657Ser
NM_005045.4:c.7970A>G MANE Select	NP_005036.2:p.Asn2657Ser
NM_173054.3:c.7970A>G	NP_774959.1:p.Asn2657Ser