Canonical Allele Identifier: CA1616315813
Gene: NRSN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145677C= , CM000668.2:g.24145677C= GRCh38
NC_000006.11:g.24145905C= , CM000668.1:g.24145905C= GRCh37
NC_000006.10:g.24253884C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378491.9:c.319C= MANE Select ENSP00000367752.4:p.Gln107=
ENST00000378477.2:c.319C= ENSP00000367738.2:p.Gln107=
ENST00000378478.5:c.319C= ENSP00000367739.2:p.Gln107=
ENST00000378491.8:c.319C= ENSP00000367752.4:p.Gln107=
ENST00000468195.2:n.257-9094C=
NM_080723.4:c.319C= NP_542454.3:p.Gln107=
NM_080723.5:c.319C= MANE Select NP_542454.3:p.Gln107=