Canonical Allele Identifier: CA3654338
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs781526166
gnomAD v2: 6-24145797-G-A
gnomAD v4: 6-24145569-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145569G>A , CM000668.2:g.24145569G>A GRCh38
NC_000006.11:g.24145797G>A , CM000668.1:g.24145797G>A GRCh37
NC_000006.10:g.24253776G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378491.9:c.211G>A MANE Select ENSP00000367752.4:p.Val71Ile
ENST00000378477.2:c.211G>A ENSP00000367738.2:p.Val71Ile
ENST00000378478.5:c.211G>A ENSP00000367739.2:p.Val71Ile
ENST00000378491.8:c.211G>A ENSP00000367752.4:p.Val71Ile
ENST00000468195.2:n.257-9202G>A
NM_080723.4:c.211G>A NP_542454.3:p.Val71Ile
NM_080723.5:c.211G>A MANE Select NP_542454.3:p.Val71Ile