Canonical Allele Identifier: CA830803197

Gene: RELN

Linked Data

• dbSNP Id: rs1330012878
• gnomAD v3: 7-103535049-A-G
• gnomAD v4: 7-103535049-A-G
• MyVariant Identifiers: chr7:g.103175496A>G (hg19) ; chr7:g.103535049A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103535049A>G , CM000669.2:g.103535049A>G	GRCh38
NC_000007.13:g.103175496A>G , CM000669.1:g.103175496A>G	GRCh37
NC_000007.12:g.102962732A>G	NCBI36
NG_011877.1:g.459468T>C
NG_011877.2:g.459468T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.7349+267T>C	ENSP00000388446.3:n.7349+267T>C
ENST00000428762.6:c.7349+267T>C MANE Select	ENSP00000392423.1:n.7349+267T>C
ENST00000478148.2:n.590+267T>C
ENST00000679867.1:n.7233+267T>C
ENST00000679952.1:n.1141+267T>C
ENST00000681034.1:c.7349+267T>C	ENSP00000506075.1:n.7349+267T>C
ENST00000681315.1:n.1496T>C
ENST00000681364.1:n.598+267T>C
ENST00000343529.9:c.7349+267T>C	ENSP00000345694.5:n.7349+267T>C
ENST00000424685.2:c.7349+267T>C	ENSP00000388446.2:n.7349+267T>C
ENST00000428762.5:c.7349+267T>C	ENSP00000392423.1:n.7349+267T>C
ENST00000478148.1:n.580+267T>C
NM_005045.3:c.7349+267T>C	NP_005036.2:n.7349+267T>C
NM_173054.2:c.7349+267T>C	NP_774959.1:n.7349+267T>C
XR_927832.1:n.41+419A>G
NM_005045.4:c.7349+267T>C MANE Select	NP_005036.2:n.7349+267T>C
NM_173054.3:c.7349+267T>C	NP_774959.1:n.7349+267T>C