Canonical Allele Identifier: CA368771187

Gene: RELN

Linked Data

• MyVariant Identifiers: chr7:g.103185732C>A (hg19) ; chr7:g.103545285C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103545285C>A , CM000669.2:g.103545285C>A	GRCh38
NC_000007.13:g.103185732C>A , CM000669.1:g.103185732C>A	GRCh37
NC_000007.12:g.102972968C>A	NCBI36
NG_011877.1:g.449232G>T
NG_011877.2:g.449232G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.6362G>T	ENSP00000388446.3:p.Trp2121Leu
ENST00000428762.6:c.6362G>T MANE Select	ENSP00000392423.1:p.Trp2121Leu
ENST00000679867.1:n.6246G>T
ENST00000679952.1:n.154G>T
ENST00000681034.1:c.6362G>T	ENSP00000506075.1:p.Trp2121Leu
ENST00000681199.1:n.2130G>T
ENST00000343529.9:c.6362G>T	ENSP00000345694.5:p.Trp2121Leu
ENST00000424685.2:c.6362G>T	ENSP00000388446.2:p.Trp2121Leu
ENST00000428762.5:c.6362G>T	ENSP00000392423.1:p.Trp2121Leu
NM_005045.3:c.6362G>T	NP_005036.2:p.Trp2121Leu
NM_173054.2:c.6362G>T	NP_774959.1:p.Trp2121Leu
NM_005045.4:c.6362G>T MANE Select	NP_005036.2:p.Trp2121Leu
NM_173054.3:c.6362G>T	NP_774959.1:p.Trp2121Leu