Canonical Allele Identifier: CA2677512579

Gene: NRSN1

Linked Data

• gnomAD v4: 6-24146051-GTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24146053_24146055del , CM000668.2:g.24146053_24146055del	GRCh38
NC_000006.11:g.24146281_24146283del , CM000668.1:g.24146281_24146283del	GRCh37
NC_000006.10:g.24254260_24254262del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.*107_*109del MANE Select	ENSP00000367752.4:n.*107_*109del
ENST00000378478.5:c.*107_*109del	ENSP00000367739.2:n.*107_*109del
ENST00000378491.8:c.*107_*109del	ENSP00000367752.4:n.*107_*109del
ENST00000468195.2:n.257-8718_257-8716del
NM_080723.4:c.*107_*109del	NP_542454.3:n.*107_*109del
NM_080723.5:c.*107_*109del MANE Select	NP_542454.3:n.*107_*109del