Canonical Allele Identifier: CA10627851

Gene: RELN

Linked Data

• ClinVar Variation Id: 358430
• ClinVar RCV Id: RCV000313866 ; RCV001534523 ; RCV004544683
• dbSNP Id: rs55656324
• gnomAD v3: 7-103989356-TGCCGCC-T
• gnomAD v4: 7-103989356-TGCCGCC-T
• MyVariant Identifiers: chr7:g.103629804_103629809del (hg19) ; chr7:g.103989357_103989362del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103989377_103989382del , CM000669.2:g.103989377_103989382del	GRCh38
NC_000007.13:g.103629824_103629829del , CM000669.1:g.103629824_103629829del	GRCh37
NC_000007.12:g.103417060_103417065del	NCBI36
NG_011877.1:g.5155_5160del
NG_011877.2:g.5155_5160del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.-6_-1del	ENSP00000388446.3:n.-6_-1del
ENST00000428762.6:c.-6_-1del MANE Select	ENSP00000392423.1:n.-6_-1del
ENST00000473457.2:n.259_264del
ENST00000679689.1:n.155_160del
ENST00000681034.1:c.-6_-1del	ENSP00000506075.1:n.-6_-1del
ENST00000681182.1:n.246_251del
ENST00000681401.1:n.271_276del
ENST00000343529.9:c.-6_-1del	ENSP00000345694.5:n.-6_-1del
ENST00000424685.2:c.-6_-1del	ENSP00000388446.2:n.-6_-1del
ENST00000428762.5:c.-6_-1del	ENSP00000392423.1:n.-6_-1del
NM_005045.3:c.-6_-1del	NP_005036.2:n.-6_-1del
NM_173054.2:c.-6_-1del	NP_774959.1:n.-6_-1del
NM_005045.4:c.-6_-1del MANE Select	NP_005036.2:n.-6_-1del
NM_173054.3:c.-6_-1del	NP_774959.1:n.-6_-1del