Canonical Allele Identifier: CA363276656
Gene: NRSN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145612T>A , CM000668.2:g.24145612T>A GRCh38
NC_000006.11:g.24145840T>A , CM000668.1:g.24145840T>A GRCh37
NC_000006.10:g.24253819T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.254T>A MANE Select ENSP00000367752.4:p.Leu85His
ENST00000378477.2:c.254T>A ENSP00000367738.2:p.Leu85His
ENST00000378478.5:c.254T>A ENSP00000367739.2:p.Leu85His
ENST00000378491.8:c.254T>A ENSP00000367752.4:p.Leu85His
ENST00000468195.2:n.257-9159T>A
NM_080723.4:c.254T>A NP_542454.3:p.Leu85His
NM_080723.5:c.254T>A MANE Select NP_542454.3:p.Leu85His