Canonical Allele Identifier: CA1730843270
Gene: RELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103678498_103678499delinsAT , CM000669.2:g.103678498_103678499delinsAT GRCh38
NC_000007.13:g.103318945_103318946delinsAT , CM000669.1:g.103318945_103318946delinsAT GRCh37
NC_000007.12:g.103106181_103106182delinsAT NCBI36
NG_011877.1:g.316018_316019delinsAT
NG_011877.2:g.316018_316019delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000424685.3:c.1289+3617_1289+3618delinsAT ENSP00000388446.3:n.1289+3617_1289+3618delinsAT
ENST00000428762.6:c.1289+3617_1289+3618delinsAT MANE Select ENSP00000392423.1:n.1289+3617_1289+3618delinsAT
ENST00000473457.2:n.1553+3617_1553+3618delinsAT
ENST00000679867.1:n.1173+3617_1173+3618delinsAT
ENST00000680712.1:n.1006+3617_1006+3618delinsAT
ENST00000681034.1:c.1289+3617_1289+3618delinsAT ENSP00000506075.1:n.1289+3617_1289+3618delinsAT
ENST00000681931.1:n.1173+3617_1173+3618delinsAT
ENST00000343529.9:c.1289+3617_1289+3618delinsAT ENSP00000345694.5:n.1289+3617_1289+3618delinsAT
ENST00000424685.2:c.1289+3617_1289+3618delinsAT ENSP00000388446.2:n.1289+3617_1289+3618delinsAT
ENST00000428762.5:c.1289+3617_1289+3618delinsAT ENSP00000392423.1:n.1289+3617_1289+3618delinsAT
NM_005045.3:c.1289+3617_1289+3618delinsAT NP_005036.2:n.1289+3617_1289+3618delinsAT
NM_173054.2:c.1289+3617_1289+3618delinsAT NP_774959.1:n.1289+3617_1289+3618delinsAT
NM_005045.4:c.1289+3617_1289+3618delinsAT MANE Select NP_005036.2:n.1289+3617_1289+3618delinsAT
NM_173054.3:c.1289+3617_1289+3618delinsAT NP_774959.1:n.1289+3617_1289+3618delinsAT