Canonical Allele Identifier: CA1105330296

Gene: RELN

Linked Data

• gnomAD v3: 7-103535008-G-T
• gnomAD v4: 7-103535008-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103535008G>T , CM000669.2:g.103535008G>T	GRCh38
NC_000007.13:g.103175455G>T , CM000669.1:g.103175455G>T	GRCh37
NC_000007.12:g.102962691G>T	NCBI36
NG_011877.1:g.459509C>A
NG_011877.2:g.459509C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.7349+308C>A	ENSP00000388446.3:n.7349+308C>A
ENST00000428762.6:c.7349+308C>A MANE Select	ENSP00000392423.1:n.7349+308C>A
ENST00000478148.2:n.590+308C>A
ENST00000679867.1:n.7233+308C>A
ENST00000679952.1:n.1141+308C>A
ENST00000681034.1:c.7349+308C>A	ENSP00000506075.1:n.7349+308C>A
ENST00000681315.1:n.1537C>A
ENST00000681364.1:n.598+308C>A
ENST00000343529.9:c.7349+308C>A	ENSP00000345694.5:n.7349+308C>A
ENST00000424685.2:c.7349+308C>A	ENSP00000388446.2:n.7349+308C>A
ENST00000428762.5:c.7349+308C>A	ENSP00000392423.1:n.7349+308C>A
ENST00000478148.1:n.580+308C>A
NM_005045.3:c.7349+308C>A	NP_005036.2:n.7349+308C>A
NM_173054.2:c.7349+308C>A	NP_774959.1:n.7349+308C>A
XR_927832.1:n.41+378G>T
NM_005045.4:c.7349+308C>A MANE Select	NP_005036.2:n.7349+308C>A
NM_173054.3:c.7349+308C>A	NP_774959.1:n.7349+308C>A