Canonical Allele Identifier: CA2501028925

Gene: NRSN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145320_24145321insG , CM000668.2:g.24145320_24145321insG	GRCh38
NC_000006.11:g.24145548_24145549insG , CM000668.1:g.24145548_24145549insG	GRCh37
NC_000006.10:g.24253527_24253528insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.190-228_190-227insG MANE Select	ENSP00000367752.4:n.190-228_190-227insG
ENST00000378477.2:c.190-228_190-227insG	ENSP00000367738.2:n.190-228_190-227insG
ENST00000378478.5:c.190-228_190-227insG	ENSP00000367739.2:n.190-228_190-227insG
ENST00000378491.8:c.190-228_190-227insG	ENSP00000367752.4:n.190-228_190-227insG
ENST00000468195.2:n.257-9451_257-9450insG
NM_080723.4:c.190-228_190-227insG	NP_542454.3:n.190-228_190-227insG
NM_080723.5:c.190-228_190-227insG MANE Select	NP_542454.3:n.190-228_190-227insG