Canonical Allele Identifier: CA1616315740
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1581554268
gnomAD v4: 6-24145503-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145503G>A , CM000668.2:g.24145503G>A GRCh38
NC_000006.11:g.24145731G>A , CM000668.1:g.24145731G>A GRCh37
NC_000006.10:g.24253710G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.190-45G>A MANE Select ENSP00000367752.4:n.190-45G>A
ENST00000378477.2:c.190-45G>A ENSP00000367738.2:n.190-45G>A
ENST00000378478.5:c.190-45G>A ENSP00000367739.2:n.190-45G>A
ENST00000378491.8:c.190-45G>A ENSP00000367752.4:n.190-45G>A
ENST00000468195.2:n.257-9268G>A
NM_080723.4:c.190-45G>A NP_542454.3:n.190-45G>A
NM_080723.5:c.190-45G>A MANE Select NP_542454.3:n.190-45G>A
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