Canonical Allele Identifier: CA1616315957

Gene: NRSN1

Linked Data

• dbSNP Id: rs1760297956
• gnomAD v3: 6-24145992-T-TA
• gnomAD v4: 6-24145992-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145997dup , CM000668.2:g.24145997dup	GRCh38
NC_000006.11:g.24146225dup , CM000668.1:g.24146225dup	GRCh37
NC_000006.10:g.24254204dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.*51dup MANE Select	ENSP00000367752.4:n.*51dup
ENST00000378478.5:c.*51dup	ENSP00000367739.2:n.*51dup
ENST00000378491.8:c.*51dup	ENSP00000367752.4:n.*51dup
ENST00000468195.2:n.257-8774dup
NM_080723.4:c.*51dup	NP_542454.3:n.*51dup
NM_080723.5:c.*51dup MANE Select	NP_542454.3:n.*51dup