Canonical Allele Identifier: CA1616315624

Gene: NRSN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145251_24145253delinsTTA , CM000668.2:g.24145251_24145253delinsTTA	GRCh38
NC_000006.11:g.24145479_24145481delinsTTA , CM000668.1:g.24145479_24145481delinsTTA	GRCh37
NC_000006.10:g.24253458_24253460delinsTTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.190-297_190-295delinsTTA MANE Select	ENSP00000367752.4:n.190-297_190-295delinsTTA
ENST00000378477.2:c.190-297_190-295delinsTTA	ENSP00000367738.2:n.190-297_190-295delinsTTA
ENST00000378478.5:c.190-297_190-295delinsTTA	ENSP00000367739.2:n.190-297_190-295delinsTTA
ENST00000378491.8:c.190-297_190-295delinsTTA	ENSP00000367752.4:n.190-297_190-295delinsTTA
ENST00000468195.2:n.257-9520_257-9518delinsTTA
NM_080723.4:c.190-297_190-295delinsTTA	NP_542454.3:n.190-297_190-295delinsTTA
NM_080723.5:c.190-297_190-295delinsTTA MANE Select	NP_542454.3:n.190-297_190-295delinsTTA