Canonical Allele Identifier: CA566217935
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1554140730
gnomAD v2: 6-24145451-T-TTATATATATCTTTAGATAATATAAAGATTA
gnomAD v3: 6-24145223-T-TTATATATATCTTTAGATAATATAAAGATTA
gnomAD v4: 6-24145223-T-TTATATATATCTTTAGATAATATAAAGATTA
MyVariant Identifiers: chr6:g.24145451_24145452insTATATATATCTTTAGATAATATAAAGATTA (hg19) chr6:g.24145223_24145224insTATATATATCTTTAGATAATATAAAGATTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145242_24145271dup , CM000668.2:g.24145242_24145271dup GRCh38
NC_000006.11:g.24145470_24145499dup , CM000668.1:g.24145470_24145499dup GRCh37
NC_000006.10:g.24253449_24253478dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.190-306_190-277dup MANE Select ENSP00000367752.4:n.190-306_190-277dup
ENST00000378477.2:c.190-306_190-277dup ENSP00000367738.2:n.190-306_190-277dup
ENST00000378478.5:c.190-306_190-277dup ENSP00000367739.2:n.190-306_190-277dup
ENST00000378491.8:c.190-306_190-277dup ENSP00000367752.4:n.190-306_190-277dup
ENST00000468195.2:n.257-9529_257-9500dup
NM_080723.4:c.190-306_190-277dup NP_542454.3:n.190-306_190-277dup
NM_080723.5:c.190-306_190-277dup MANE Select NP_542454.3:n.190-306_190-277dup
Search 100 bp 5'
Search 100 bp 3'