Canonical Allele Identifier: CA363276723

Gene: NRSN1

Linked Data

• MyVariant Identifiers: chr6:g.24145872G>A (hg19) ; chr6:g.24145644G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145644G>A , CM000668.2:g.24145644G>A	GRCh38
NC_000006.11:g.24145872G>A , CM000668.1:g.24145872G>A	GRCh37
NC_000006.10:g.24253851G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.286G>A MANE Select	ENSP00000367752.4:p.Ala96Thr
ENST00000378477.2:c.286G>A	ENSP00000367738.2:p.Ala96Thr
ENST00000378478.5:c.286G>A	ENSP00000367739.2:p.Ala96Thr
ENST00000378491.8:c.286G>A	ENSP00000367752.4:p.Ala96Thr
ENST00000468195.2:n.257-9127G>A
NM_080723.4:c.286G>A	NP_542454.3:p.Ala96Thr
NM_080723.5:c.286G>A MANE Select	NP_542454.3:p.Ala96Thr