Canonical Allele Identifier: CA1616316025

Gene: NRSN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24146145T= , CM000668.2:g.24146145T=	GRCh38
NC_000006.11:g.24146373T= , CM000668.1:g.24146373T=	GRCh37
NC_000006.10:g.24254352T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.*199T= MANE Select	ENSP00000367752.4:n.*199T=
ENST00000378478.5:c.*199T=	ENSP00000367739.2:n.*199T=
ENST00000378491.8:c.*199T=	ENSP00000367752.4:n.*199T=
ENST00000468195.2:n.257-8626T=
NM_080723.4:c.*199T=	NP_542454.3:n.*199T=
NM_080723.5:c.*199T= MANE Select	NP_542454.3:n.*199T=