Canonical Allele Identifier: CA823266079
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1342575796
gnomAD v3: 6-24145988-TG-T
gnomAD v4: 6-24145988-TG-T
MyVariant Identifiers: chr6:g.24146217del (hg19) chr6:g.24145989del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145990del , CM000668.2:g.24145990del GRCh38
NC_000006.11:g.24146218del , CM000668.1:g.24146218del GRCh37
NC_000006.10:g.24254197del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.*44del MANE Select ENSP00000367752.4:n.*44del
ENST00000378478.5:c.*44del ENSP00000367739.2:n.*44del
ENST00000378491.8:c.*44del ENSP00000367752.4:n.*44del
ENST00000468195.2:n.257-8781del
NM_080723.4:c.*44del NP_542454.3:n.*44del
NM_080723.5:c.*44del MANE Select NP_542454.3:n.*44del
Search 100 bp 5'
Search 100 bp 3'