Canonical Allele Identifier: CA2189589917

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601826_78601827delinsCT , CM000677.2:g.78601826_78601827delinsCT	GRCh38
NC_000015.9:g.78894168_78894169delinsCT , CM000677.1:g.78894168_78894169delinsCT	GRCh37
NC_000015.8:g.76681223_76681224delinsCT	NCBI36
NG_016143.1:g.24469_24470delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.815_816delinsAG MANE Select	ENSP00000315602.5:p.Lys272=
ENST00000326828.5:c.815_816delinsAG	ENSP00000315602.5:p.Lys272=
ENST00000348639.7:c.815_816delinsAG	ENSP00000267951.4:p.Lys272=
ENST00000558903.1:n.522_523delinsAG
ENST00000559658.5:c.815_816delinsAG	ENSP00000452896.1:p.Lys272=
NM_000743.4:c.815_816delinsAG	NP_000734.2:p.Lys272=
NM_001166694.1:c.815_816delinsAG	NP_001160166.1:p.Lys272=
NR_046313.1:n.1316_1317delinsAG
XM_006720382.1:c.614_615delinsAG	XP_006720445.1:p.Lys205=
XM_011521173.1:c.734_735delinsAG	XP_011519475.1:p.Lys245=
XM_006720382.3:c.614_615delinsAG	XP_006720445.1:p.Lys205=
NM_000743.5:c.815_816delinsAG MANE Select	NP_000734.2:p.Lys272=
NM_001166694.2:c.815_816delinsAG	NP_001160166.1:p.Lys272=
NR_046313.2:n.1017_1018delinsAG