Canonical Allele Identifier: CA2677512468

Gene: NRSN1

Linked Data

• gnomAD v4: 6-24145478-CTTGAGGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145479_24145485del , CM000668.2:g.24145479_24145485del	GRCh38
NC_000006.11:g.24145707_24145713del , CM000668.1:g.24145707_24145713del	GRCh37
NC_000006.10:g.24253686_24253692del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.190-69_190-63del MANE Select	ENSP00000367752.4:n.190-69_190-63del
ENST00000378477.2:c.190-69_190-63del	ENSP00000367738.2:n.190-69_190-63del
ENST00000378478.5:c.190-69_190-63del	ENSP00000367739.2:n.190-69_190-63del
ENST00000378491.8:c.190-69_190-63del	ENSP00000367752.4:n.190-69_190-63del
ENST00000468195.2:n.257-9292_257-9286del
NM_080723.4:c.190-69_190-63del	NP_542454.3:n.190-69_190-63del
NM_080723.5:c.190-69_190-63del MANE Select	NP_542454.3:n.190-69_190-63del