Canonical Allele Identifier: CA393585604
Gene: CHRNA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78602011T>C , CM000677.2:g.78602011T>C GRCh38
NC_000015.9:g.78894353T>C , CM000677.1:g.78894353T>C GRCh37
NC_000015.8:g.76681408T>C NCBI36
NG_016143.1:g.24285A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.631A>G MANE Select ENSP00000315602.5:p.Lys211Glu
ENST00000326828.5:c.631A>G ENSP00000315602.5:p.Lys211Glu
ENST00000348639.7:c.631A>G ENSP00000267951.4:p.Lys211Glu
ENST00000558903.1:n.338A>G
ENST00000559658.5:c.631A>G ENSP00000452896.1:p.Lys211Glu
NM_000743.4:c.631A>G NP_000734.2:p.Lys211Glu
NM_001166694.1:c.631A>G NP_001160166.1:p.Lys211Glu
NR_046313.1:n.1132A>G
XM_006720382.1:c.430A>G XP_006720445.1:p.Lys144Glu
XM_011521173.1:c.550A>G XP_011519475.1:p.Lys184Glu
XM_006720382.3:c.430A>G XP_006720445.1:p.Lys144Glu
NM_000743.5:c.631A>G MANE Select NP_000734.2:p.Lys211Glu
NM_001166694.2:c.631A>G NP_001160166.1:p.Lys211Glu
NR_046313.2:n.833A>G