Canonical Allele Identifier: CA2677512564
Gene: NRSN1 HGNC NCBI

Linked Data

gnomAD v4: 6-24146037-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24146037A>G , CM000668.2:g.24146037A>G GRCh38
NC_000006.11:g.24146265A>G , CM000668.1:g.24146265A>G GRCh37
NC_000006.10:g.24254244A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.*91A>G MANE Select ENSP00000367752.4:n.*91A>G
ENST00000378478.5:c.*91A>G ENSP00000367739.2:n.*91A>G
ENST00000378491.8:c.*91A>G ENSP00000367752.4:n.*91A>G
ENST00000468195.2:n.257-8734A>G
NM_080723.4:c.*91A>G NP_542454.3:n.*91A>G
NM_080723.5:c.*91A>G MANE Select NP_542454.3:n.*91A>G
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