Canonical Allele Identifier: CA1616315919
Gene: NRSN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145923G= , CM000668.2:g.24145923G= GRCh38
NC_000006.11:g.24146151G= , CM000668.1:g.24146151G= GRCh37
NC_000006.10:g.24254130G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.565G= MANE Select ENSP00000367752.4:p.Val189=
ENST00000378478.5:c.565G= ENSP00000367739.2:p.Val189=
ENST00000378491.8:c.565G= ENSP00000367752.4:p.Val189=
ENST00000468195.2:n.257-8848G=
NM_080723.4:c.565G= NP_542454.3:p.Val189=
NM_080723.5:c.565G= MANE Select NP_542454.3:p.Val189=
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