Canonical Allele Identifier: CA2189589913

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601825_78601828delinsCCTT , CM000677.2:g.78601825_78601828delinsCCTT	GRCh38
NC_000015.9:g.78894167_78894170delinsCCTT , CM000677.1:g.78894167_78894170delinsCCTT	GRCh37
NC_000015.8:g.76681222_76681225delinsCCTT	NCBI36
NG_016143.1:g.24468_24471delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.814_817delinsAAGG MANE Select	ENSP00000315602.5:p.Lys272=
ENST00000326828.5:c.814_817delinsAAGG	ENSP00000315602.5:p.Lys272=
ENST00000348639.7:c.814_817delinsAAGG	ENSP00000267951.4:p.Lys272=
ENST00000558903.1:n.521_524delinsAAGG
ENST00000559658.5:c.814_817delinsAAGG	ENSP00000452896.1:p.Lys272=
NM_000743.4:c.814_817delinsAAGG	NP_000734.2:p.Lys272=
NM_001166694.1:c.814_817delinsAAGG	NP_001160166.1:p.Lys272=
NR_046313.1:n.1315_1318delinsAAGG
XM_006720382.1:c.613_616delinsAAGG	XP_006720445.1:p.Lys205=
XM_011521173.1:c.733_736delinsAAGG	XP_011519475.1:p.Lys245=
XM_006720382.3:c.613_616delinsAAGG	XP_006720445.1:p.Lys205=
NM_000743.5:c.814_817delinsAAGG MANE Select	NP_000734.2:p.Lys272=
NM_001166694.2:c.814_817delinsAAGG	NP_001160166.1:p.Lys272=
NR_046313.2:n.1016_1019delinsAAGG