Canonical Allele Identifier: CA2578541559

Gene: NRSN1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145986C>G , CM000668.2:g.24145986C>G	GRCh38
NC_000006.11:g.24146214C>G , CM000668.1:g.24146214C>G	GRCh37
NC_000006.10:g.24254193C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.*40C>G MANE Select	ENSP00000367752.4:n.*40C>G
ENST00000378478.5:c.*40C>G	ENSP00000367739.2:n.*40C>G
ENST00000378491.8:c.*40C>G	ENSP00000367752.4:n.*40C>G
ENST00000468195.2:n.257-8785C>G
NM_080723.4:c.*40C>G	NP_542454.3:n.*40C>G
NM_080723.5:c.*40C>G MANE Select	NP_542454.3:n.*40C>G