Canonical Allele Identifier: CA1772813610

Gene: CHRNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463202_27463203delinsTC , CM000670.2:g.27463202_27463203delinsTC	GRCh38
NC_000008.10:g.27320719_27320720delinsTC , CM000670.1:g.27320719_27320720delinsTC	GRCh37
NC_000008.9:g.27376636_27376637delinsTC	NCBI36
NG_015827.1:g.21094_21095delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1240_1241delinsGA MANE Select	ENSP00000385026.1:p.Glu414=
ENST00000240132.7:c.1195_1196delinsGA	ENSP00000240132.2:p.Glu399=
ENST00000407991.2:c.1240_1241delinsGA	ENSP00000385026.1:p.Glu414=
ENST00000520600.1:n.290-1449_290-1448delinsGA
ENST00000520933.7:c.1174_1175delinsGA	ENSP00000429616.2:p.Glu392=
ENST00000523695.5:c.*642_*643delinsGA	ENSP00000430612.1:n.*642_*643delinsGA
NM_000742.3:c.1240_1241delinsGA	NP_000733.2:p.Glu414=
NM_001282455.1:c.1195_1196delinsGA	NP_001269384.1:p.Glu399=
XM_005273397.1:c.763_764delinsGA	XP_005273454.1:p.Glu255=
XM_006716282.1:c.1240_1241delinsGA	XP_006716345.1:p.Glu414=
XM_011544388.1:c.1240_1241delinsGA	XP_011542690.1:p.Glu414=
XM_011544389.1:c.646_647delinsGA	XP_011542691.1:p.Glu216=
NM_001347705.1:c.763_764delinsGA	NP_001334634.1:p.Glu255=
NM_001347706.1:c.763_764delinsGA	NP_001334635.1:p.Glu255=
NM_001347707.1:c.646_647delinsGA	NP_001334636.1:p.Glu216=
NM_001347708.1:c.646_647delinsGA	NP_001334637.1:p.Glu216=
XM_011544389.2:c.646_647delinsGA	XP_011542691.1:p.Glu216=
NM_000742.4:c.1240_1241delinsGA MANE Select	NP_000733.2:p.Glu414=
NM_001282455.2:c.1195_1196delinsGA	NP_001269384.1:p.Glu399=
NM_001347705.2:c.763_764delinsGA	NP_001334634.1:p.Glu255=
NM_001347706.2:c.763_764delinsGA	NP_001334635.1:p.Glu255=
NM_001347707.2:c.646_647delinsGA	NP_001334636.1:p.Glu216=
NM_001347708.2:c.646_647delinsGA	NP_001334637.1:p.Glu216=