Canonical Allele Identifier: CA1616315652

Gene: NRSN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145285_24145286delinsTA , CM000668.2:g.24145285_24145286delinsTA	GRCh38
NC_000006.11:g.24145513_24145514delinsTA , CM000668.1:g.24145513_24145514delinsTA	GRCh37
NC_000006.10:g.24253492_24253493delinsTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.190-263_190-262delinsTA MANE Select	ENSP00000367752.4:n.190-263_190-262delinsTA
ENST00000378477.2:c.190-263_190-262delinsTA	ENSP00000367738.2:n.190-263_190-262delinsTA
ENST00000378478.5:c.190-263_190-262delinsTA	ENSP00000367739.2:n.190-263_190-262delinsTA
ENST00000378491.8:c.190-263_190-262delinsTA	ENSP00000367752.4:n.190-263_190-262delinsTA
ENST00000468195.2:n.257-9486_257-9485delinsTA
NM_080723.4:c.190-263_190-262delinsTA	NP_542454.3:n.190-263_190-262delinsTA
NM_080723.5:c.190-263_190-262delinsTA MANE Select	NP_542454.3:n.190-263_190-262delinsTA