Canonical Allele Identifier: CA393580602
Community Standard Title: NM_000743.5(CHRNA3):c.1460G>C (p.Cys487Ser)
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78596662C>G , CM000677.2:g.78596662C>G GRCh38
NC_000015.9:g.78889004C>G , CM000677.1:g.78889004C>G GRCh37
NC_000015.8:g.76676059C>G NCBI36
NG_016143.1:g.29634G>C
NG_023328.1:g.36143C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000743.5:c.1460G>C MANE Select NP_000734.2:p.Cys487Ser
ENST00000326828.6:c.1460G>C MANE Select ENSP00000315602.5:p.Cys487Ser
NM_000743.4:c.1460G>C NP_000734.2:p.Cys487Ser
NM_001166694.1:c.1390-3471G>C NP_001160166.1:n.1390-3471G>C
NM_001166694.2:c.1390-3471G>C NP_001160166.1:n.1390-3471G>C
NR_046313.1:n.1961G>C
NR_046313.2:n.1662G>C
ENST00000326828.5:c.1460G>C ENSP00000315602.5:p.Cys487Ser
ENST00000348639.7:c.1390-3471G>C ENSP00000267951.4:n.1390-3471G>C
ENST00000559002.5:n.71G>C
ENST00000559658.5:c.1460G>C ENSP00000452896.1:p.Cys487Ser
XM_006720382.1:c.1259G>C XP_006720445.1:p.Cys420Ser
XM_006720382.3:c.1259G>C XP_006720445.1:p.Cys420Ser
XM_011521173.1:c.1379G>C XP_011519475.1:p.Cys460Ser