Canonical Allele Identifier: CA1772813863

Gene: CHRNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463301T= , CM000670.2:g.27463301T=	GRCh38
NC_000008.10:g.27320818T= , CM000670.1:g.27320818T=	GRCh37
NC_000008.9:g.27376735T=	NCBI36
NG_015827.1:g.20996A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1142A= MANE Select	ENSP00000385026.1:p.Asn381=
ENST00000240132.7:c.1097A=	ENSP00000240132.2:p.Asn366=
ENST00000407991.2:c.1142A=	ENSP00000385026.1:p.Asn381=
ENST00000520600.1:n.290-1547A=
ENST00000520933.7:c.1076A=	ENSP00000429616.2:p.Asn359=
ENST00000523695.5:c.*544A=	ENSP00000430612.1:n.*544A=
NM_000742.3:c.1142A=	NP_000733.2:p.Asn381=
NM_001282455.1:c.1097A=	NP_001269384.1:p.Asn366=
XM_005273397.1:c.665A=	XP_005273454.1:p.Asn222=
XM_006716282.1:c.1142A=	XP_006716345.1:p.Asn381=
XM_011544388.1:c.1142A=	XP_011542690.1:p.Asn381=
XM_011544389.1:c.548A=	XP_011542691.1:p.Asn183=
NM_001347705.1:c.665A=	NP_001334634.1:p.Asn222=
NM_001347706.1:c.665A=	NP_001334635.1:p.Asn222=
NM_001347707.1:c.548A=	NP_001334636.1:p.Asn183=
NM_001347708.1:c.548A=	NP_001334637.1:p.Asn183=
XM_011544389.2:c.548A=	XP_011542691.1:p.Asn183=
NM_000742.4:c.1142A= MANE Select	NP_000733.2:p.Asn381=
NM_001282455.2:c.1097A=	NP_001269384.1:p.Asn366=
NM_001347705.2:c.665A=	NP_001334634.1:p.Asn222=
NM_001347706.2:c.665A=	NP_001334635.1:p.Asn222=
NM_001347707.2:c.548A=	NP_001334636.1:p.Asn183=
NM_001347708.2:c.548A=	NP_001334637.1:p.Asn183=