Canonical Allele Identifier: CA7684249

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78596754_78596758del , CM000677.2:g.78596754_78596758del	GRCh38
NC_000015.9:g.78889096_78889100del , CM000677.1:g.78889096_78889100del	GRCh37
NC_000015.8:g.76676151_76676155del	NCBI36
NG_016143.1:g.29542_29546del
NG_023328.1:g.36235_36239del

Transcript Alleles

HGVS	Amino-acid Change
NM_000743.5:c.1390-22_1390-18del MANE Select	NP_000734.2:n.1390-22_1390-18del
ENST00000326828.6:c.1390-22_1390-18del MANE Select	ENSP00000315602.5:n.1390-22_1390-18del
NM_000743.4:c.1390-22_1390-18del	NP_000734.2:n.1390-22_1390-18del
NM_001166694.1:c.1390-3563_1390-3559del	NP_001160166.1:n.1390-3563_1390-3559del
NM_001166694.2:c.1390-3563_1390-3559del	NP_001160166.1:n.1390-3563_1390-3559del
NR_046313.1:n.1891-22_1891-18del
NR_046313.2:n.1592-22_1592-18del
ENST00000326828.5:c.1390-22_1390-18del	ENSP00000315602.5:n.1390-22_1390-18del
ENST00000348639.7:c.1390-3563_1390-3559del	ENSP00000267951.4:n.1390-3563_1390-3559del
ENST00000559658.5:c.1390-22_1390-18del	ENSP00000452896.1:n.1390-22_1390-18del
XM_006720382.1:c.1189-22_1189-18del	XP_006720445.1:n.1189-22_1189-18del
XM_006720382.3:c.1189-22_1189-18del	XP_006720445.1:n.1189-22_1189-18del
XM_011521173.1:c.1309-22_1309-18del	XP_011519475.1:n.1309-22_1309-18del