Canonical Allele Identifier: CA363276728
Gene: NRSN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24145873C>A (hg19) chr6:g.24145645C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145645C>A , CM000668.2:g.24145645C>A GRCh38
NC_000006.11:g.24145873C>A , CM000668.1:g.24145873C>A GRCh37
NC_000006.10:g.24253852C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.287C>A MANE Select ENSP00000367752.4:p.Ala96Asp
ENST00000378477.2:c.287C>A ENSP00000367738.2:p.Ala96Asp
ENST00000378478.5:c.287C>A ENSP00000367739.2:p.Ala96Asp
ENST00000378491.8:c.287C>A ENSP00000367752.4:p.Ala96Asp
ENST00000468195.2:n.257-9126C>A
NM_080723.4:c.287C>A NP_542454.3:p.Ala96Asp
NM_080723.5:c.287C>A MANE Select NP_542454.3:p.Ala96Asp
Search 100 bp 5'
Search 100 bp 3'