Canonical Allele Identifier: CA136618284

Gene: NRSN1

Linked Data

• dbSNP Id: rs1038335753
• gnomAD v3: 6-24145250-A-ATT
• gnomAD v4: 6-24145250-A-ATT
• MyVariant Identifiers: chr6:g.24145478_24145479insTT (hg19) ; chr6:g.24145250_24145251insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145251_24145252dup , CM000668.2:g.24145251_24145252dup	GRCh38
NC_000006.11:g.24145479_24145480dup , CM000668.1:g.24145479_24145480dup	GRCh37
NC_000006.10:g.24253458_24253459dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.190-297_190-296dup MANE Select	ENSP00000367752.4:n.190-297_190-296dup
ENST00000378477.2:c.190-297_190-296dup	ENSP00000367738.2:n.190-297_190-296dup
ENST00000378478.5:c.190-297_190-296dup	ENSP00000367739.2:n.190-297_190-296dup
ENST00000378491.8:c.190-297_190-296dup	ENSP00000367752.4:n.190-297_190-296dup
ENST00000468195.2:n.257-9520_257-9519dup
NM_080723.4:c.190-297_190-296dup	NP_542454.3:n.190-297_190-296dup
NM_080723.5:c.190-297_190-296dup MANE Select	NP_542454.3:n.190-297_190-296dup