Canonical Allele Identifier: CA363277285
Gene: NRSN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145902A>T , CM000668.2:g.24145902A>T GRCh38
NC_000006.11:g.24146130A>T , CM000668.1:g.24146130A>T GRCh37
NC_000006.10:g.24254109A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.544A>T MANE Select ENSP00000367752.4:p.Thr182Ser
ENST00000378478.5:c.544A>T ENSP00000367739.2:p.Thr182Ser
ENST00000378491.8:c.544A>T ENSP00000367752.4:p.Thr182Ser
ENST00000468195.2:n.257-8869A>T
NM_080723.4:c.544A>T NP_542454.3:p.Thr182Ser
NM_080723.5:c.544A>T MANE Select NP_542454.3:p.Thr182Ser