Canonical Allele Identifier: CA1616315703

Gene: NRSN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145400_24145404delinsAAATT , CM000668.2:g.24145400_24145404delinsAAATT	GRCh38
NC_000006.11:g.24145628_24145632delinsAAATT , CM000668.1:g.24145628_24145632delinsAAATT	GRCh37
NC_000006.10:g.24253607_24253611delinsAAATT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.190-148_190-144delinsAAATT MANE Select	ENSP00000367752.4:n.190-148_190-144delinsAAATT
ENST00000378477.2:c.190-148_190-144delinsAAATT	ENSP00000367738.2:n.190-148_190-144delinsAAATT
ENST00000378478.5:c.190-148_190-144delinsAAATT	ENSP00000367739.2:n.190-148_190-144delinsAAATT
ENST00000378491.8:c.190-148_190-144delinsAAATT	ENSP00000367752.4:n.190-148_190-144delinsAAATT
ENST00000468195.2:n.257-9371_257-9367delinsAAATT
NM_080723.4:c.190-148_190-144delinsAAATT	NP_542454.3:n.190-148_190-144delinsAAATT
NM_080723.5:c.190-148_190-144delinsAAATT MANE Select	NP_542454.3:n.190-148_190-144delinsAAATT