Canonical Allele Identifier: CA363276740
Gene: NRSN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24145879T>A (hg19) chr6:g.24145651T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145651T>A , CM000668.2:g.24145651T>A GRCh38
NC_000006.11:g.24145879T>A , CM000668.1:g.24145879T>A GRCh37
NC_000006.10:g.24253858T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.293T>A MANE Select ENSP00000367752.4:p.Phe98Tyr
ENST00000378477.2:c.293T>A ENSP00000367738.2:p.Phe98Tyr
ENST00000378478.5:c.293T>A ENSP00000367739.2:p.Phe98Tyr
ENST00000378491.8:c.293T>A ENSP00000367752.4:p.Phe98Tyr
ENST00000468195.2:n.257-9120T>A
NM_080723.4:c.293T>A NP_542454.3:p.Phe98Tyr
NM_080723.5:c.293T>A MANE Select NP_542454.3:p.Phe98Tyr
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