Canonical Allele Identifier: CA1730775562
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103535085A= , CM000669.2:g.103535085A= GRCh38
NC_000007.13:g.103175532A= , CM000669.1:g.103175532A= GRCh37
NC_000007.12:g.102962768A= NCBI36
NG_011877.1:g.459432T=
NG_011877.2:g.459432T=

Transcript Alleles

HGVS Amino-acid change
ENST00000424685.3:c.7349+231T= ENSP00000388446.3:n.7349+231T=
ENST00000428762.6:c.7349+231T= MANE Select ENSP00000392423.1:n.7349+231T=
ENST00000478148.2:n.590+231T=
ENST00000679867.1:n.7233+231T=
ENST00000679952.1:n.1141+231T=
ENST00000681034.1:c.7349+231T= ENSP00000506075.1:n.7349+231T=
ENST00000681315.1:n.1460T=
ENST00000681364.1:n.598+231T=
ENST00000343529.9:c.7349+231T= ENSP00000345694.5:n.7349+231T=
ENST00000424685.2:c.7349+231T= ENSP00000388446.2:n.7349+231T=
ENST00000428762.5:c.7349+231T= ENSP00000392423.1:n.7349+231T=
ENST00000478148.1:n.580+231T=
NM_005045.3:c.7349+231T= NP_005036.2:n.7349+231T=
NM_173054.2:c.7349+231T= NP_774959.1:n.7349+231T=
XR_927832.1:n.41+455A=
NM_005045.4:c.7349+231T= MANE Select NP_005036.2:n.7349+231T=
NM_173054.3:c.7349+231T= NP_774959.1:n.7349+231T=