Canonical Allele Identifier: CA823265071
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1298007065

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145403_24145406del , CM000668.2:g.24145403_24145406del GRCh38
NC_000006.11:g.24145631_24145634del , CM000668.1:g.24145631_24145634del GRCh37
NC_000006.10:g.24253610_24253613del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.190-145_190-142del MANE Select ENSP00000367752.4:n.190-145_190-142del
ENST00000378477.2:c.190-145_190-142del ENSP00000367738.2:n.190-145_190-142del
ENST00000378478.5:c.190-145_190-142del ENSP00000367739.2:n.190-145_190-142del
ENST00000378491.8:c.190-145_190-142del ENSP00000367752.4:n.190-145_190-142del
ENST00000468195.2:n.257-9368_257-9365del
NM_080723.4:c.190-145_190-142del NP_542454.3:n.190-145_190-142del
NM_080723.5:c.190-145_190-142del MANE Select NP_542454.3:n.190-145_190-142del