Canonical Allele Identifier: CA1616315690

Gene: NRSN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145368_24145372delinsTAGAA , CM000668.2:g.24145368_24145372delinsTAGAA	GRCh38
NC_000006.11:g.24145596_24145600delinsTAGAA , CM000668.1:g.24145596_24145600delinsTAGAA	GRCh37
NC_000006.10:g.24253575_24253579delinsTAGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.190-180_190-176delinsTAGAA MANE Select	ENSP00000367752.4:n.190-180_190-176delinsTAGAA
ENST00000378477.2:c.190-180_190-176delinsTAGAA	ENSP00000367738.2:n.190-180_190-176delinsTAGAA
ENST00000378478.5:c.190-180_190-176delinsTAGAA	ENSP00000367739.2:n.190-180_190-176delinsTAGAA
ENST00000378491.8:c.190-180_190-176delinsTAGAA	ENSP00000367752.4:n.190-180_190-176delinsTAGAA
ENST00000468195.2:n.257-9403_257-9399delinsTAGAA
NM_080723.4:c.190-180_190-176delinsTAGAA	NP_542454.3:n.190-180_190-176delinsTAGAA
NM_080723.5:c.190-180_190-176delinsTAGAA MANE Select	NP_542454.3:n.190-180_190-176delinsTAGAA