Canonical Allele Identifier: CA1105334553

Gene: RELN

Linked Data

• dbSNP Id: rs1830279320
• gnomAD v3: 7-103545658-T-TG
• gnomAD v4: 7-103545658-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103545658_103545659insG , CM000669.2:g.103545658_103545659insG	GRCh38
NC_000007.13:g.103186105_103186106insG , CM000669.1:g.103186105_103186106insG	GRCh37
NC_000007.12:g.102973341_102973342insG	NCBI36
NG_011877.1:g.448858_448859insC
NG_011877.2:g.448858_448859insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.6303-315_6303-314insC	ENSP00000388446.3:n.6303-315_6303-314insC
ENST00000428762.6:c.6303-315_6303-314insC MANE Select	ENSP00000392423.1:n.6303-315_6303-314insC
ENST00000679867.1:n.6187-315_6187-314insC
ENST00000679952.1:n.95-315_95-314insC
ENST00000681034.1:c.6303-315_6303-314insC	ENSP00000506075.1:n.6303-315_6303-314insC
ENST00000681199.1:n.2071-315_2071-314insC
ENST00000343529.9:c.6303-315_6303-314insC	ENSP00000345694.5:n.6303-315_6303-314insC
ENST00000424685.2:c.6303-315_6303-314insC	ENSP00000388446.2:n.6303-315_6303-314insC
ENST00000428762.5:c.6303-315_6303-314insC	ENSP00000392423.1:n.6303-315_6303-314insC
NM_005045.3:c.6303-315_6303-314insC	NP_005036.2:n.6303-315_6303-314insC
NM_173054.2:c.6303-315_6303-314insC	NP_774959.1:n.6303-315_6303-314insC
NM_005045.4:c.6303-315_6303-314insC MANE Select	NP_005036.2:n.6303-315_6303-314insC
NM_173054.3:c.6303-315_6303-314insC	NP_774959.1:n.6303-315_6303-314insC