Canonical Allele Identifier: CA448963004

Gene: NRSN1

Linked Data

• MyVariant Identifiers: chr6:g.24145793T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145565T>G , CM000668.2:g.24145565T>G	GRCh38
NC_000006.11:g.24145793T>G , CM000668.1:g.24145793T>G	GRCh37
NC_000006.10:g.24253772T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.207T>G MANE Select	ENSP00000367752.4:p.Gly69=
ENST00000378477.2:c.207T>G	ENSP00000367738.2:p.Gly69=
ENST00000378478.5:c.207T>G	ENSP00000367739.2:p.Gly69=
ENST00000378491.8:c.207T>G	ENSP00000367752.4:p.Gly69=
ENST00000468195.2:n.257-9206T>G
NM_080723.4:c.207T>G	NP_542454.3:p.Gly69=
NM_080723.5:c.207T>G MANE Select	NP_542454.3:p.Gly69=