Canonical Allele Identifier: CA363276854
Gene: NRSN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24145930A>T (hg19) chr6:g.24145702A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145702A>T , CM000668.2:g.24145702A>T GRCh38
NC_000006.11:g.24145930A>T , CM000668.1:g.24145930A>T GRCh37
NC_000006.10:g.24253909A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.344A>T MANE Select ENSP00000367752.4:p.Tyr115Phe
ENST00000378477.2:c.344A>T ENSP00000367738.2:p.Tyr115Phe
ENST00000378478.5:c.344A>T ENSP00000367739.2:p.Tyr115Phe
ENST00000378491.8:c.344A>T ENSP00000367752.4:p.Tyr115Phe
ENST00000468195.2:n.257-9069A>T
NM_080723.4:c.344A>T NP_542454.3:p.Tyr115Phe
NM_080723.5:c.344A>T MANE Select NP_542454.3:p.Tyr115Phe
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