Canonical Allele Identifier: CA163938440

Gene: RELN

Linked Data

• dbSNP Id: rs1056810718
• MyVariant Identifiers: chr7:g.103175472T>G (hg19) ; chr7:g.103535025T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.103535025T>G , CM000669.2:g.103535025T>G	GRCh38
NC_000007.13:g.103175472T>G , CM000669.1:g.103175472T>G	GRCh37
NC_000007.12:g.102962708T>G	NCBI36
NG_011877.1:g.459492A>C
NG_011877.2:g.459492A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000424685.3:c.7349+291A>C	ENSP00000388446.3:n.7349+291A>C
ENST00000428762.6:c.7349+291A>C MANE Select	ENSP00000392423.1:n.7349+291A>C
ENST00000478148.2:n.590+291A>C
ENST00000679867.1:n.7233+291A>C
ENST00000679952.1:n.1141+291A>C
ENST00000681034.1:c.7349+291A>C	ENSP00000506075.1:n.7349+291A>C
ENST00000681315.1:n.1520A>C
ENST00000681364.1:n.598+291A>C
ENST00000343529.9:c.7349+291A>C	ENSP00000345694.5:n.7349+291A>C
ENST00000424685.2:c.7349+291A>C	ENSP00000388446.2:n.7349+291A>C
ENST00000428762.5:c.7349+291A>C	ENSP00000392423.1:n.7349+291A>C
ENST00000478148.1:n.580+291A>C
NM_005045.3:c.7349+291A>C	NP_005036.2:n.7349+291A>C
NM_173054.2:c.7349+291A>C	NP_774959.1:n.7349+291A>C
XR_927832.1:n.41+395T>G
NM_005045.4:c.7349+291A>C MANE Select	NP_005036.2:n.7349+291A>C
NM_173054.3:c.7349+291A>C	NP_774959.1:n.7349+291A>C