Canonical Allele Identifier: CA1616315922
Gene: NRSN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145929C= , CM000668.2:g.24145929C= GRCh38
NC_000006.11:g.24146157C= , CM000668.1:g.24146157C= GRCh37
NC_000006.10:g.24254136C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.571C= MANE Select ENSP00000367752.4:p.Pro191=
ENST00000378478.5:c.571C= ENSP00000367739.2:p.Pro191=
ENST00000378491.8:c.571C= ENSP00000367752.4:p.Pro191=
ENST00000468195.2:n.257-8842C=
NM_080723.4:c.571C= NP_542454.3:p.Pro191=
NM_080723.5:c.571C= MANE Select NP_542454.3:p.Pro191=
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