Canonical Allele Identifier: CA2677512583
Gene: NRSN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24146053_24146054insCCAAATC , CM000668.2:g.24146053_24146054insCCAAATC GRCh38
NC_000006.11:g.24146281_24146282insCCAAATC , CM000668.1:g.24146281_24146282insCCAAATC GRCh37
NC_000006.10:g.24254260_24254261insCCAAATC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.*107_*108insCCAAATC MANE Select ENSP00000367752.4:n.*107_*108insCCAAATC
ENST00000378478.5:c.*107_*108insCCAAATC ENSP00000367739.2:n.*107_*108insCCAAATC
ENST00000378491.8:c.*107_*108insCCAAATC ENSP00000367752.4:n.*107_*108insCCAAATC
ENST00000468195.2:n.257-8718_257-8717insCCAAATC
NM_080723.4:c.*107_*108insCCAAATC NP_542454.3:n.*107_*108insCCAAATC
NM_080723.5:c.*107_*108insCCAAATC MANE Select NP_542454.3:n.*107_*108insCCAAATC