Canonical Allele Identifier: CA363277003
Gene: NRSN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24146002T>G (hg19) chr6:g.24145774T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145774T>G , CM000668.2:g.24145774T>G GRCh38
NC_000006.11:g.24146002T>G , CM000668.1:g.24146002T>G GRCh37
NC_000006.10:g.24253981T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.416T>G MANE Select ENSP00000367752.4:p.Phe139Cys
ENST00000378477.2:c.416T>G ENSP00000367738.2:p.Phe139Cys
ENST00000378478.5:c.416T>G ENSP00000367739.2:p.Phe139Cys
ENST00000378491.8:c.416T>G ENSP00000367752.4:p.Phe139Cys
ENST00000468195.2:n.257-8997T>G
NM_080723.4:c.416T>G NP_542454.3:p.Phe139Cys
NM_080723.5:c.416T>G MANE Select NP_542454.3:p.Phe139Cys
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