Canonical Allele Identifier: CA1616315837
Gene: NRSN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145736_24145747delinsAGGCACGTCCAT , CM000668.2:g.24145736_24145747delinsAGGCACGTCCAT GRCh38
NC_000006.11:g.24145964_24145975delinsAGGCACGTCCAT , CM000668.1:g.24145964_24145975delinsAGGCACGTCCAT GRCh37
NC_000006.10:g.24253943_24253954delinsAGGCACGTCCAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.378_389delinsAGGCACGTCCAT MANE Select ENSP00000367752.4:p.Gly126=
ENST00000378477.2:c.378_389delinsAGGCACGTCCAT ENSP00000367738.2:p.Gly126=
ENST00000378478.5:c.378_389delinsAGGCACGTCCAT ENSP00000367739.2:p.Gly126=
ENST00000378491.8:c.378_389delinsAGGCACGTCCAT ENSP00000367752.4:p.Gly126=
ENST00000468195.2:n.257-9035_257-9024delinsAGGCACGTCCAT
NM_080723.4:c.378_389delinsAGGCACGTCCAT NP_542454.3:p.Gly126=
NM_080723.5:c.378_389delinsAGGCACGTCCAT MANE Select NP_542454.3:p.Gly126=