Canonical Allele Identifier: CA1616315662

Gene: NRSN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145299_24145301delinsTAA , CM000668.2:g.24145299_24145301delinsTAA	GRCh38
NC_000006.11:g.24145527_24145529delinsTAA , CM000668.1:g.24145527_24145529delinsTAA	GRCh37
NC_000006.10:g.24253506_24253508delinsTAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.190-249_190-247delinsTAA MANE Select	ENSP00000367752.4:n.190-249_190-247delinsTAA
ENST00000378477.2:c.190-249_190-247delinsTAA	ENSP00000367738.2:n.190-249_190-247delinsTAA
ENST00000378478.5:c.190-249_190-247delinsTAA	ENSP00000367739.2:n.190-249_190-247delinsTAA
ENST00000378491.8:c.190-249_190-247delinsTAA	ENSP00000367752.4:n.190-249_190-247delinsTAA
ENST00000468195.2:n.257-9472_257-9470delinsTAA
NM_080723.4:c.190-249_190-247delinsTAA	NP_542454.3:n.190-249_190-247delinsTAA
NM_080723.5:c.190-249_190-247delinsTAA MANE Select	NP_542454.3:n.190-249_190-247delinsTAA