Canonical Allele Identifier: CA830825134

Gene: RELN

Linked Data

• dbSNP Id: rs1176417349
• gnomAD v3: 7-103985355-C-CT
• gnomAD v4: 7-103985355-C-CT
• MyVariant Identifiers: chr7:g.103625802_103625803insT (hg19) ; chr7:g.103985355_103985356insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103985356dup , CM000669.2:g.103985356dup	GRCh38
NC_000007.13:g.103625803dup , CM000669.1:g.103625803dup	GRCh37
NC_000007.12:g.103413039dup	NCBI36
NG_011877.1:g.9161dup
NG_011877.2:g.9161dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.226+3775dup	ENSP00000388446.3:n.226+3775dup
ENST00000428762.6:c.226+3775dup MANE Select	ENSP00000392423.1:n.226+3775dup
ENST00000473457.2:n.490+3775dup
ENST00000679689.1:n.386+3775dup
ENST00000679867.1:n.110+3775dup
ENST00000680712.1:n.40+3775dup
ENST00000681034.1:c.226+3775dup	ENSP00000506075.1:n.226+3775dup
ENST00000681182.1:n.477+3775dup
ENST00000681401.1:n.502+3775dup
ENST00000681931.1:n.110+3775dup
ENST00000343529.9:c.226+3775dup	ENSP00000345694.5:n.226+3775dup
ENST00000424685.2:c.226+3775dup	ENSP00000388446.2:n.226+3775dup
ENST00000428762.5:c.226+3775dup	ENSP00000392423.1:n.226+3775dup
NM_005045.3:c.226+3775dup	NP_005036.2:n.226+3775dup
NM_173054.2:c.226+3775dup	NP_774959.1:n.226+3775dup
NM_005045.4:c.226+3775dup MANE Select	NP_005036.2:n.226+3775dup
NM_173054.3:c.226+3775dup	NP_774959.1:n.226+3775dup