Canonical Allele Identifier: CA2711296775

Gene: NRSN1

Linked Data

• dbSNP Id: rs2113719481

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24145953T>C , CM000668.2:g.24145953T>C	GRCh38
NC_000006.11:g.24146181T>C , CM000668.1:g.24146181T>C	GRCh37
NC_000006.10:g.24254160T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378491.9:c.*7T>C MANE Select	ENSP00000367752.4:n.*7T>C
ENST00000378478.5:c.*7T>C	ENSP00000367739.2:n.*7T>C
ENST00000378491.8:c.*7T>C	ENSP00000367752.4:n.*7T>C
ENST00000468195.2:n.257-8818T>C
NM_080723.4:c.*7T>C	NP_542454.3:n.*7T>C
NM_080723.5:c.*7T>C MANE Select	NP_542454.3:n.*7T>C