Canonical Allele Identifier: CA576939752

Gene: RELN

Linked Data

• dbSNP Id: rs1456764821
• gnomAD v2: 7-103186097-T-TA
• gnomAD v3: 7-103545650-T-TA
• gnomAD v4: 7-103545650-T-TA
• MyVariant Identifiers: chr7:g.103186097_103186098insA (hg19) ; chr7:g.103545650_103545651insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103545650_103545651insA , CM000669.2:g.103545650_103545651insA	GRCh38
NC_000007.13:g.103186097_103186098insA , CM000669.1:g.103186097_103186098insA	GRCh37
NC_000007.12:g.102973333_102973334insA	NCBI36
NG_011877.1:g.448866_448867insT
NG_011877.2:g.448866_448867insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.6303-307_6303-306insT	ENSP00000388446.3:n.6303-307_6303-306insT
ENST00000428762.6:c.6303-307_6303-306insT MANE Select	ENSP00000392423.1:n.6303-307_6303-306insT
ENST00000679867.1:n.6187-307_6187-306insT
ENST00000679952.1:n.95-307_95-306insT
ENST00000681034.1:c.6303-307_6303-306insT	ENSP00000506075.1:n.6303-307_6303-306insT
ENST00000681199.1:n.2071-307_2071-306insT
ENST00000343529.9:c.6303-307_6303-306insT	ENSP00000345694.5:n.6303-307_6303-306insT
ENST00000424685.2:c.6303-307_6303-306insT	ENSP00000388446.2:n.6303-307_6303-306insT
ENST00000428762.5:c.6303-307_6303-306insT	ENSP00000392423.1:n.6303-307_6303-306insT
NM_005045.3:c.6303-307_6303-306insT	NP_005036.2:n.6303-307_6303-306insT
NM_173054.2:c.6303-307_6303-306insT	NP_774959.1:n.6303-307_6303-306insT
NM_005045.4:c.6303-307_6303-306insT MANE Select	NP_005036.2:n.6303-307_6303-306insT
NM_173054.3:c.6303-307_6303-306insT	NP_774959.1:n.6303-307_6303-306insT