Canonical Allele Identifier: CA1616315851
Gene: NRSN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145768_24145769delinsCG , CM000668.2:g.24145768_24145769delinsCG GRCh38
NC_000006.11:g.24145996_24145997delinsCG , CM000668.1:g.24145996_24145997delinsCG GRCh37
NC_000006.10:g.24253975_24253976delinsCG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.410_411delinsCG MANE Select ENSP00000367752.4:p.Ser137=
ENST00000378477.2:c.410_411delinsCG ENSP00000367738.2:p.Ser137=
ENST00000378478.5:c.410_411delinsCG ENSP00000367739.2:p.Ser137=
ENST00000378491.8:c.410_411delinsCG ENSP00000367752.4:p.Ser137=
ENST00000468195.2:n.257-9003_257-9002delinsCG
NM_080723.4:c.410_411delinsCG NP_542454.3:p.Ser137=
NM_080723.5:c.410_411delinsCG MANE Select NP_542454.3:p.Ser137=