Canonical Allele Identifier: CA2677512513
Gene: NRSN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145574del , CM000668.2:g.24145574del GRCh38
NC_000006.11:g.24145802del , CM000668.1:g.24145802del GRCh37
NC_000006.10:g.24253781del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378491.9:c.216del MANE Select ENSP00000367752.4:p.Phe72LeufsTer2
ENST00000378477.2:c.216del ENSP00000367738.2:p.Phe72LeufsTer2
ENST00000378478.5:c.216del ENSP00000367739.2:p.Phe72LeufsTer2
ENST00000378491.8:c.216del ENSP00000367752.4:p.Phe72LeufsTer2
ENST00000468195.2:n.257-9197del
NM_080723.4:c.216del NP_542454.3:p.Phe72LeufsTer2
NM_080723.5:c.216del MANE Select NP_542454.3:p.Phe72LeufsTer2