Canonical Allele Identifier: CA1616315660
Gene: NRSN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145297T= , CM000668.2:g.24145297T= GRCh38
NC_000006.11:g.24145525T= , CM000668.1:g.24145525T= GRCh37
NC_000006.10:g.24253504T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.190-251T= MANE Select ENSP00000367752.4:n.190-251T=
ENST00000378477.2:c.190-251T= ENSP00000367738.2:n.190-251T=
ENST00000378478.5:c.190-251T= ENSP00000367739.2:n.190-251T=
ENST00000378491.8:c.190-251T= ENSP00000367752.4:n.190-251T=
ENST00000468195.2:n.257-9474T=
NM_080723.4:c.190-251T= NP_542454.3:n.190-251T=
NM_080723.5:c.190-251T= MANE Select NP_542454.3:n.190-251T=
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