Canonical Allele Identifier: CA1772813906

Gene: CHRNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463327G= , CM000670.2:g.27463327G=	GRCh38
NC_000008.10:g.27320844G= , CM000670.1:g.27320844G=	GRCh37
NC_000008.9:g.27376761G=	NCBI36
NG_015827.1:g.20970C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1116C= MANE Select	ENSP00000385026.1:p.Gly372=
ENST00000240132.7:c.1071C=	ENSP00000240132.2:p.Gly357=
ENST00000407991.2:c.1116C=	ENSP00000385026.1:p.Gly372=
ENST00000520600.1:n.290-1573C=
ENST00000520933.7:c.1050C=	ENSP00000429616.2:p.Gly350=
ENST00000523695.5:c.*518C=	ENSP00000430612.1:n.*518C=
NM_000742.3:c.1116C=	NP_000733.2:p.Gly372=
NM_001282455.1:c.1071C=	NP_001269384.1:p.Gly357=
XM_005273397.1:c.639C=	XP_005273454.1:p.Gly213=
XM_006716282.1:c.1116C=	XP_006716345.1:p.Gly372=
XM_011544388.1:c.1116C=	XP_011542690.1:p.Gly372=
XM_011544389.1:c.522C=	XP_011542691.1:p.Gly174=
NM_001347705.1:c.639C=	NP_001334634.1:p.Gly213=
NM_001347706.1:c.639C=	NP_001334635.1:p.Gly213=
NM_001347707.1:c.522C=	NP_001334636.1:p.Gly174=
NM_001347708.1:c.522C=	NP_001334637.1:p.Gly174=
XM_011544389.2:c.522C=	XP_011542691.1:p.Gly174=
NM_000742.4:c.1116C= MANE Select	NP_000733.2:p.Gly372=
NM_001282455.2:c.1071C=	NP_001269384.1:p.Gly357=
NM_001347705.2:c.639C=	NP_001334634.1:p.Gly213=
NM_001347706.2:c.639C=	NP_001334635.1:p.Gly213=
NM_001347707.2:c.522C=	NP_001334636.1:p.Gly174=
NM_001347708.2:c.522C=	NP_001334637.1:p.Gly174=