Canonical Allele Identifier: CA566217933
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1318455157
gnomAD v2: 6-24145426-A-AATATATCTTTAGATAATATAAAGATTAT
gnomAD v3: 6-24145198-A-AATATATCTTTAGATAATATAAAGATTAT
gnomAD v4: 6-24145198-A-AATATATCTTTAGATAATATAAAGATTAT
MyVariant Identifiers: chr6:g.24145454_24145455insATATATCTTTAGATAATATAAAGATTAT (hg19) chr6:g.24145226_24145227insATATATCTTTAGATAATATAAAGATTAT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145233_24145260dup , CM000668.2:g.24145233_24145260dup GRCh38
NC_000006.11:g.24145461_24145488dup , CM000668.1:g.24145461_24145488dup GRCh37
NC_000006.10:g.24253440_24253467dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.190-315_190-288dup MANE Select ENSP00000367752.4:n.190-315_190-288dup
ENST00000378477.2:c.190-315_190-288dup ENSP00000367738.2:n.190-315_190-288dup
ENST00000378478.5:c.190-315_190-288dup ENSP00000367739.2:n.190-315_190-288dup
ENST00000378491.8:c.190-315_190-288dup ENSP00000367752.4:n.190-315_190-288dup
ENST00000468195.2:n.257-9538_257-9511dup
NM_080723.4:c.190-315_190-288dup NP_542454.3:n.190-315_190-288dup
NM_080723.5:c.190-315_190-288dup MANE Select NP_542454.3:n.190-315_190-288dup
Search 100 bp 5'
Search 100 bp 3'