Canonical Allele Identifier: CA1730794740

Gene: RELN

Linked Data

• dbSNP Id: rs1830901931
• gnomAD v4: 7-103572348-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103572348T>A , CM000669.2:g.103572348T>A	GRCh38
NC_000007.13:g.103212795T>A , CM000669.1:g.103212795T>A	GRCh37
NC_000007.12:g.103000031T>A	NCBI36
NG_011877.1:g.422169A>T
NG_011877.2:g.422169A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424685.3:c.4512-88A>T	ENSP00000388446.3:n.4512-88A>T
ENST00000428762.6:c.4512-88A>T MANE Select	ENSP00000392423.1:n.4512-88A>T
ENST00000679867.1:n.4396-88A>T
ENST00000680706.1:n.2215-88A>T
ENST00000681034.1:c.4512-88A>T	ENSP00000506075.1:n.4512-88A>T
ENST00000343529.9:c.4512-88A>T	ENSP00000345694.5:n.4512-88A>T
ENST00000424685.2:c.4512-88A>T	ENSP00000388446.2:n.4512-88A>T
ENST00000428762.5:c.4512-88A>T	ENSP00000392423.1:n.4512-88A>T
NM_005045.3:c.4512-88A>T	NP_005036.2:n.4512-88A>T
NM_173054.2:c.4512-88A>T	NP_774959.1:n.4512-88A>T
NM_005045.4:c.4512-88A>T MANE Select	NP_005036.2:n.4512-88A>T
NM_173054.3:c.4512-88A>T	NP_774959.1:n.4512-88A>T