Canonical Allele Identifier: CA650738588

Gene: NRSN1

Linked Data

• COSMIC: COSN17955555

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24146013C>G , CM000668.2:g.24146013C>G	GRCh38
NC_000006.11:g.24146241C>G , CM000668.1:g.24146241C>G	GRCh37
NC_000006.10:g.24254220C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.*67C>G MANE Select	ENSP00000367752.4:n.*67C>G
ENST00000378478.5:c.*67C>G	ENSP00000367739.2:n.*67C>G
ENST00000378491.8:c.*67C>G	ENSP00000367752.4:n.*67C>G
ENST00000468195.2:n.257-8758C>G
NM_080723.4:c.*67C>G	NP_542454.3:n.*67C>G
NM_080723.5:c.*67C>G MANE Select	NP_542454.3:n.*67C>G