Canonical Allele Identifier: CA2514493938

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103535087A>C , CM000669.2:g.103535087A>C	GRCh38
NC_000007.13:g.103175534A>C , CM000669.1:g.103175534A>C	GRCh37
NC_000007.12:g.102962770A>C	NCBI36
NG_011877.1:g.459430T>G
NG_011877.2:g.459430T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.7349+229T>G	ENSP00000388446.3:n.7349+229T>G
ENST00000428762.6:c.7349+229T>G MANE Select	ENSP00000392423.1:n.7349+229T>G
ENST00000478148.2:n.590+229T>G
ENST00000679867.1:n.7233+229T>G
ENST00000679952.1:n.1141+229T>G
ENST00000681034.1:c.7349+229T>G	ENSP00000506075.1:n.7349+229T>G
ENST00000681315.1:n.1458T>G
ENST00000681364.1:n.598+229T>G
ENST00000343529.9:c.7349+229T>G	ENSP00000345694.5:n.7349+229T>G
ENST00000424685.2:c.7349+229T>G	ENSP00000388446.2:n.7349+229T>G
ENST00000428762.5:c.7349+229T>G	ENSP00000392423.1:n.7349+229T>G
ENST00000478148.1:n.580+229T>G
NM_005045.3:c.7349+229T>G	NP_005036.2:n.7349+229T>G
NM_173054.2:c.7349+229T>G	NP_774959.1:n.7349+229T>G
XR_927832.1:n.41+457A>C
NM_005045.4:c.7349+229T>G MANE Select	NP_005036.2:n.7349+229T>G
NM_173054.3:c.7349+229T>G	NP_774959.1:n.7349+229T>G