Canonical Allele Identifier: CA566217937
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs201221669
gnomAD v2: 6-24145479-T-TTA
gnomAD v3: 6-24145251-T-TTA
gnomAD v4: 6-24145251-T-TTA
MyVariant Identifiers: chr6:g.24145481_24145482insTA (hg19) chr6:g.24145479_24145480insTA (hg19) chr6:g.24145253_24145254insTA (hg38) chr6:g.24145251_24145252insTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145261_24145262dup , CM000668.2:g.24145261_24145262dup GRCh38
NC_000006.11:g.24145489_24145490dup , CM000668.1:g.24145489_24145490dup GRCh37
NC_000006.10:g.24253468_24253469dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.190-287_190-286dup MANE Select ENSP00000367752.4:n.190-287_190-286dup
ENST00000378477.2:c.190-287_190-286dup ENSP00000367738.2:n.190-287_190-286dup
ENST00000378478.5:c.190-287_190-286dup ENSP00000367739.2:n.190-287_190-286dup
ENST00000378491.8:c.190-287_190-286dup ENSP00000367752.4:n.190-287_190-286dup
ENST00000468195.2:n.257-9510_257-9509dup
NM_080723.4:c.190-287_190-286dup NP_542454.3:n.190-287_190-286dup
NM_080723.5:c.190-287_190-286dup MANE Select NP_542454.3:n.190-287_190-286dup
Search 100 bp 5'
Search 100 bp 3'