Canonical Allele Identifier: CA363276668
Gene: NRSN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24145848C>G (hg19) chr6:g.24145620C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145620C>G , CM000668.2:g.24145620C>G GRCh38
NC_000006.11:g.24145848C>G , CM000668.1:g.24145848C>G GRCh37
NC_000006.10:g.24253827C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.262C>G MANE Select ENSP00000367752.4:p.Pro88Ala
ENST00000378477.2:c.262C>G ENSP00000367738.2:p.Pro88Ala
ENST00000378478.5:c.262C>G ENSP00000367739.2:p.Pro88Ala
ENST00000378491.8:c.262C>G ENSP00000367752.4:p.Pro88Ala
ENST00000468195.2:n.257-9151C>G
NM_080723.4:c.262C>G NP_542454.3:p.Pro88Ala
NM_080723.5:c.262C>G MANE Select NP_542454.3:p.Pro88Ala
Search 100 bp 5'
Search 100 bp 3'