Canonical Allele Identifier: CA363277244
Gene: NRSN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145884G>A , CM000668.2:g.24145884G>A GRCh38
NC_000006.11:g.24146112G>A , CM000668.1:g.24146112G>A GRCh37
NC_000006.10:g.24254091G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.526G>A MANE Select ENSP00000367752.4:p.Glu176Lys
ENST00000378478.5:c.526G>A ENSP00000367739.2:p.Glu176Lys
ENST00000378491.8:c.526G>A ENSP00000367752.4:p.Glu176Lys
ENST00000468195.2:n.257-8887G>A
NM_080723.4:c.526G>A NP_542454.3:p.Glu176Lys
NM_080723.5:c.526G>A MANE Select NP_542454.3:p.Glu176Lys