Canonical Allele Identifier: CA1616315788
Gene: NRSN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145621C= , CM000668.2:g.24145621C= GRCh38
NC_000006.11:g.24145849C= , CM000668.1:g.24145849C= GRCh37
NC_000006.10:g.24253828C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.263C= MANE Select ENSP00000367752.4:p.Pro88=
ENST00000378477.2:c.263C= ENSP00000367738.2:p.Pro88=
ENST00000378478.5:c.263C= ENSP00000367739.2:p.Pro88=
ENST00000378491.8:c.263C= ENSP00000367752.4:p.Pro88=
ENST00000468195.2:n.257-9150C=
NM_080723.4:c.263C= NP_542454.3:p.Pro88=
NM_080723.5:c.263C= MANE Select NP_542454.3:p.Pro88=
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