Canonical Allele Identifier: CA363276795
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1425772312
gnomAD v2: 6-24145905-C-T
gnomAD v3: 6-24145677-C-T
gnomAD v4: 6-24145677-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145677C>T , CM000668.2:g.24145677C>T GRCh38
NC_000006.11:g.24145905C>T , CM000668.1:g.24145905C>T GRCh37
NC_000006.10:g.24253884C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378491.9:c.319C>T MANE Select ENSP00000367752.4:p.Gln107Ter
ENST00000378477.2:c.319C>T ENSP00000367738.2:p.Gln107Ter
ENST00000378478.5:c.319C>T ENSP00000367739.2:p.Gln107Ter
ENST00000378491.8:c.319C>T ENSP00000367752.4:p.Gln107Ter
ENST00000468195.2:n.257-9094C>T
NM_080723.4:c.319C>T NP_542454.3:p.Gln107Ter
NM_080723.5:c.319C>T MANE Select NP_542454.3:p.Gln107Ter