Canonical Allele Identifier: CA1616315654

Gene: NRSN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145288_24145289delinsCT , CM000668.2:g.24145288_24145289delinsCT	GRCh38
NC_000006.11:g.24145516_24145517delinsCT , CM000668.1:g.24145516_24145517delinsCT	GRCh37
NC_000006.10:g.24253495_24253496delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.190-260_190-259delinsCT MANE Select	ENSP00000367752.4:n.190-260_190-259delinsCT
ENST00000378477.2:c.190-260_190-259delinsCT	ENSP00000367738.2:n.190-260_190-259delinsCT
ENST00000378478.5:c.190-260_190-259delinsCT	ENSP00000367739.2:n.190-260_190-259delinsCT
ENST00000378491.8:c.190-260_190-259delinsCT	ENSP00000367752.4:n.190-260_190-259delinsCT
ENST00000468195.2:n.257-9483_257-9482delinsCT
NM_080723.4:c.190-260_190-259delinsCT	NP_542454.3:n.190-260_190-259delinsCT
NM_080723.5:c.190-260_190-259delinsCT MANE Select	NP_542454.3:n.190-260_190-259delinsCT