Canonical Allele Identifier: CA1616315941
Gene: NRSN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145972G= , CM000668.2:g.24145972G= GRCh38
NC_000006.11:g.24146200G= , CM000668.1:g.24146200G= GRCh37
NC_000006.10:g.24254179G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.*26G= MANE Select ENSP00000367752.4:n.*26G=
ENST00000378478.5:c.*26G= ENSP00000367739.2:n.*26G=
ENST00000378491.8:c.*26G= ENSP00000367752.4:n.*26G=
ENST00000468195.2:n.257-8799G=
NM_080723.4:c.*26G= NP_542454.3:n.*26G=
NM_080723.5:c.*26G= MANE Select NP_542454.3:n.*26G=