Canonical Allele Identifier: CA1616315987
Gene: NRSN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24146057A= , CM000668.2:g.24146057A= GRCh38
NC_000006.11:g.24146285A= , CM000668.1:g.24146285A= GRCh37
NC_000006.10:g.24254264A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.*111A= MANE Select ENSP00000367752.4:n.*111A=
ENST00000378478.5:c.*111A= ENSP00000367739.2:n.*111A=
ENST00000378491.8:c.*111A= ENSP00000367752.4:n.*111A=
ENST00000468195.2:n.257-8714A=
NM_080723.4:c.*111A= NP_542454.3:n.*111A=
NM_080723.5:c.*111A= MANE Select NP_542454.3:n.*111A=