Canonical Allele Identifier: CA2578541548
Gene: NRSN1 HGNC NCBI

Linked Data

gnomAD v4: 6-24145488-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145488C>A , CM000668.2:g.24145488C>A GRCh38
NC_000006.11:g.24145716C>A , CM000668.1:g.24145716C>A GRCh37
NC_000006.10:g.24253695C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.190-60C>A MANE Select ENSP00000367752.4:n.190-60C>A
ENST00000378477.2:c.190-60C>A ENSP00000367738.2:n.190-60C>A
ENST00000378478.5:c.190-60C>A ENSP00000367739.2:n.190-60C>A
ENST00000378491.8:c.190-60C>A ENSP00000367752.4:n.190-60C>A
ENST00000468195.2:n.257-9283C>A
NM_080723.4:c.190-60C>A NP_542454.3:n.190-60C>A
NM_080723.5:c.190-60C>A MANE Select NP_542454.3:n.190-60C>A
Search 100 bp 5'
Search 100 bp 3'