Canonical Allele Identifier: CA2189590157

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601916_78601917delinsCA , CM000677.2:g.78601916_78601917delinsCA	GRCh38
NC_000015.9:g.78894258_78894259delinsCA , CM000677.1:g.78894258_78894259delinsCA	GRCh37
NC_000015.8:g.76681313_76681314delinsCA	NCBI36
NG_016143.1:g.24379_24380delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.725_726delinsTG MANE Select	ENSP00000315602.5:p.Leu242=
ENST00000326828.5:c.725_726delinsTG	ENSP00000315602.5:p.Leu242=
ENST00000348639.7:c.725_726delinsTG	ENSP00000267951.4:p.Leu242=
ENST00000558903.1:n.432_433delinsTG
ENST00000559658.5:c.725_726delinsTG	ENSP00000452896.1:p.Leu242=
NM_000743.4:c.725_726delinsTG	NP_000734.2:p.Leu242=
NM_001166694.1:c.725_726delinsTG	NP_001160166.1:p.Leu242=
NR_046313.1:n.1226_1227delinsTG
XM_006720382.1:c.524_525delinsTG	XP_006720445.1:p.Leu175=
XM_011521173.1:c.644_645delinsTG	XP_011519475.1:p.Leu215=
XM_006720382.3:c.524_525delinsTG	XP_006720445.1:p.Leu175=
NM_000743.5:c.725_726delinsTG MANE Select	NP_000734.2:p.Leu242=
NM_001166694.2:c.725_726delinsTG	NP_001160166.1:p.Leu242=
NR_046313.2:n.927_928delinsTG