Canonical Allele Identifier: CA448962999

Gene: NRSN1

Linked Data

• MyVariant Identifiers: chr6:g.24145790A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145562A>G , CM000668.2:g.24145562A>G	GRCh38
NC_000006.11:g.24145790A>G , CM000668.1:g.24145790A>G	GRCh37
NC_000006.10:g.24253769A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.204A>G MANE Select	ENSP00000367752.4:p.Ser68=
ENST00000378477.2:c.204A>G	ENSP00000367738.2:p.Ser68=
ENST00000378478.5:c.204A>G	ENSP00000367739.2:p.Ser68=
ENST00000378491.8:c.204A>G	ENSP00000367752.4:p.Ser68=
ENST00000468195.2:n.257-9209A>G
NM_080723.4:c.204A>G	NP_542454.3:p.Ser68=
NM_080723.5:c.204A>G MANE Select	NP_542454.3:p.Ser68=