Canonical Allele Identifier: CA4422302

Gene: RELN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103661538A>G , CM000669.2:g.103661538A>G	GRCh38
NC_000007.13:g.103301985A>G , CM000669.1:g.103301985A>G	GRCh37
NC_000007.12:g.103089221A>G	NCBI36
NG_011877.1:g.332979T>C
NG_011877.2:g.332979T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.1290-11T>C	ENSP00000388446.3:n.1290-11T>C
ENST00000428762.6:c.1290-11T>C MANE Select	ENSP00000392423.1:n.1290-11T>C
ENST00000473457.2:n.1554-11T>C
ENST00000679867.1:n.1174-11T>C
ENST00000680712.1:n.1007-11T>C
ENST00000681034.1:c.1290-11T>C	ENSP00000506075.1:n.1290-11T>C
ENST00000681931.1:n.1174-11T>C
ENST00000343529.9:c.1290-11T>C	ENSP00000345694.5:n.1290-11T>C
ENST00000424685.2:c.1290-11T>C	ENSP00000388446.2:n.1290-11T>C
ENST00000428762.5:c.1290-11T>C	ENSP00000392423.1:n.1290-11T>C
NM_005045.3:c.1290-11T>C	NP_005036.2:n.1290-11T>C
NM_173054.2:c.1290-11T>C	NP_774959.1:n.1290-11T>C
NM_005045.4:c.1290-11T>C MANE Select	NP_005036.2:n.1290-11T>C
NM_173054.3:c.1290-11T>C	NP_774959.1:n.1290-11T>C