Canonical Allele Identifier: CA576939743

Gene: RELN

Linked Data

• dbSNP Id: rs1271388006
• gnomAD v2: 7-103186087-T-TA
• gnomAD v3: 7-103545640-T-TA
• gnomAD v4: 7-103545640-T-TA
• MyVariant Identifiers: chr7:g.103186087_103186088insA (hg19) ; chr7:g.103545640_103545641insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103545640_103545641insA , CM000669.2:g.103545640_103545641insA	GRCh38
NC_000007.13:g.103186087_103186088insA , CM000669.1:g.103186087_103186088insA	GRCh37
NC_000007.12:g.102973323_102973324insA	NCBI36
NG_011877.1:g.448876_448877insT
NG_011877.2:g.448876_448877insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.6303-297_6303-296insT	ENSP00000388446.3:n.6303-297_6303-296insT
ENST00000428762.6:c.6303-297_6303-296insT MANE Select	ENSP00000392423.1:n.6303-297_6303-296insT
ENST00000679867.1:n.6187-297_6187-296insT
ENST00000679952.1:n.95-297_95-296insT
ENST00000681034.1:c.6303-297_6303-296insT	ENSP00000506075.1:n.6303-297_6303-296insT
ENST00000681199.1:n.2071-297_2071-296insT
ENST00000343529.9:c.6303-297_6303-296insT	ENSP00000345694.5:n.6303-297_6303-296insT
ENST00000424685.2:c.6303-297_6303-296insT	ENSP00000388446.2:n.6303-297_6303-296insT
ENST00000428762.5:c.6303-297_6303-296insT	ENSP00000392423.1:n.6303-297_6303-296insT
NM_005045.3:c.6303-297_6303-296insT	NP_005036.2:n.6303-297_6303-296insT
NM_173054.2:c.6303-297_6303-296insT	NP_774959.1:n.6303-297_6303-296insT
NM_005045.4:c.6303-297_6303-296insT MANE Select	NP_005036.2:n.6303-297_6303-296insT
NM_173054.3:c.6303-297_6303-296insT	NP_774959.1:n.6303-297_6303-296insT