Canonical Allele Identifier: CA1616315990

Gene: NRSN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24146063G= , CM000668.2:g.24146063G=	GRCh38
NC_000006.11:g.24146291G= , CM000668.1:g.24146291G=	GRCh37
NC_000006.10:g.24254270G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.*117G= MANE Select	ENSP00000367752.4:n.*117G=
ENST00000378478.5:c.*117G=	ENSP00000367739.2:n.*117G=
ENST00000378491.8:c.*117G=	ENSP00000367752.4:n.*117G=
ENST00000468195.2:n.257-8708G=
NM_080723.4:c.*117G=	NP_542454.3:n.*117G=
NM_080723.5:c.*117G= MANE Select	NP_542454.3:n.*117G=