Canonical Allele Identifier: CA1616315907
Gene: NRSN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145889A= , CM000668.2:g.24145889A= GRCh38
NC_000006.11:g.24146117A= , CM000668.1:g.24146117A= GRCh37
NC_000006.10:g.24254096A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.531A= MANE Select ENSP00000367752.4:p.Thr177=
ENST00000378478.5:c.531A= ENSP00000367739.2:p.Thr177=
ENST00000378491.8:c.531A= ENSP00000367752.4:p.Thr177=
ENST00000468195.2:n.257-8882A=
NM_080723.4:c.531A= NP_542454.3:p.Thr177=
NM_080723.5:c.531A= MANE Select NP_542454.3:p.Thr177=
Search 100 bp 5'
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