Canonical Allele Identifier: CA136618315
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs902569432

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145682dup , CM000668.2:g.24145682dup GRCh38
NC_000006.11:g.24145910dup , CM000668.1:g.24145910dup GRCh37
NC_000006.10:g.24253889dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378491.9:c.324dup MANE Select ENSP00000367752.4:p.Asn109Ter
ENST00000378477.2:c.324dup ENSP00000367738.2:p.Asn109Ter
ENST00000378478.5:c.324dup ENSP00000367739.2:p.Asn109Ter
ENST00000378491.8:c.324dup ENSP00000367752.4:p.Asn109Ter
ENST00000468195.2:n.257-9089dup
NM_080723.4:c.324dup NP_542454.3:p.Asn109Ter
NM_080723.5:c.324dup MANE Select NP_542454.3:p.Asn109Ter