Canonical Allele Identifier: CA2677512618
Gene: NRSN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24146098del , CM000668.2:g.24146098del GRCh38
NC_000006.11:g.24146326del , CM000668.1:g.24146326del GRCh37
NC_000006.10:g.24254305del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.*152del MANE Select ENSP00000367752.4:n.*152del
ENST00000378478.5:c.*152del ENSP00000367739.2:n.*152del
ENST00000378491.8:c.*152del ENSP00000367752.4:n.*152del
ENST00000468195.2:n.257-8673del
NM_080723.4:c.*152del NP_542454.3:n.*152del
NM_080723.5:c.*152del MANE Select NP_542454.3:n.*152del