Canonical Allele Identifier: CA363277009
Gene: NRSN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145777T>A , CM000668.2:g.24145777T>A GRCh38
NC_000006.11:g.24146005T>A , CM000668.1:g.24146005T>A GRCh37
NC_000006.10:g.24253984T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.419T>A MANE Select ENSP00000367752.4:p.Val140Glu
ENST00000378477.2:c.419T>A ENSP00000367738.2:p.Val140Glu
ENST00000378478.5:c.419T>A ENSP00000367739.2:p.Val140Glu
ENST00000378491.8:c.419T>A ENSP00000367752.4:p.Val140Glu
ENST00000468195.2:n.257-8994T>A
NM_080723.4:c.419T>A NP_542454.3:p.Val140Glu
NM_080723.5:c.419T>A MANE Select NP_542454.3:p.Val140Glu