Canonical Allele Identifier: CA823265018

Gene: NRSN1

Linked Data

• dbSNP Id: rs1428480952
• MyVariant Identifiers: chr6:g.24145517del (hg19) ; chr6:g.24145289del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145291del , CM000668.2:g.24145291del	GRCh38
NC_000006.11:g.24145519del , CM000668.1:g.24145519del	GRCh37
NC_000006.10:g.24253498del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.190-257del MANE Select	ENSP00000367752.4:n.190-257del
ENST00000378477.2:c.190-257del	ENSP00000367738.2:n.190-257del
ENST00000378478.5:c.190-257del	ENSP00000367739.2:n.190-257del
ENST00000378491.8:c.190-257del	ENSP00000367752.4:n.190-257del
ENST00000468195.2:n.257-9480del
NM_080723.4:c.190-257del	NP_542454.3:n.190-257del
NM_080723.5:c.190-257del MANE Select	NP_542454.3:n.190-257del