Canonical Allele Identifier: CA363276834

Gene: NRSN1

Linked Data

• MyVariant Identifiers: chr6:g.24145923G>T (hg19) ; chr6:g.24145695G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145695G>T , CM000668.2:g.24145695G>T	GRCh38
NC_000006.11:g.24145923G>T , CM000668.1:g.24145923G>T	GRCh37
NC_000006.10:g.24253902G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.337G>T MANE Select	ENSP00000367752.4:p.Asp113Tyr
ENST00000378477.2:c.337G>T	ENSP00000367738.2:p.Asp113Tyr
ENST00000378478.5:c.337G>T	ENSP00000367739.2:p.Asp113Tyr
ENST00000378491.8:c.337G>T	ENSP00000367752.4:p.Asp113Tyr
ENST00000468195.2:n.257-9076G>T
NM_080723.4:c.337G>T	NP_542454.3:p.Asp113Tyr
NM_080723.5:c.337G>T MANE Select	NP_542454.3:p.Asp113Tyr