Canonical Allele Identifier: CA1616315908
Gene: NRSN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145892G= , CM000668.2:g.24145892G= GRCh38
NC_000006.11:g.24146120G= , CM000668.1:g.24146120G= GRCh37
NC_000006.10:g.24254099G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.534G= MANE Select ENSP00000367752.4:p.Lys178=
ENST00000378478.5:c.534G= ENSP00000367739.2:p.Lys178=
ENST00000378491.8:c.534G= ENSP00000367752.4:p.Lys178=
ENST00000468195.2:n.257-8879G=
NM_080723.4:c.534G= NP_542454.3:p.Lys178=
NM_080723.5:c.534G= MANE Select NP_542454.3:p.Lys178=
Search 100 bp 5'
Search 100 bp 3'