Canonical Allele Identifier: CA2677512581

Gene: NRSN1

Linked Data

• gnomAD v4: 6-24146052-T-TCAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24146052_24146053insCAAC , CM000668.2:g.24146052_24146053insCAAC	GRCh38
NC_000006.11:g.24146280_24146281insCAAC , CM000668.1:g.24146280_24146281insCAAC	GRCh37
NC_000006.10:g.24254259_24254260insCAAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.*106_*107insCAAC MANE Select	ENSP00000367752.4:n.*106_*107insCAAC
ENST00000378478.5:c.*106_*107insCAAC	ENSP00000367739.2:n.*106_*107insCAAC
ENST00000378491.8:c.*106_*107insCAAC	ENSP00000367752.4:n.*106_*107insCAAC
ENST00000468195.2:n.257-8719_257-8718insCAAC
NM_080723.4:c.*106_*107insCAAC	NP_542454.3:n.*106_*107insCAAC
NM_080723.5:c.*106_*107insCAAC MANE Select	NP_542454.3:n.*106_*107insCAAC