Canonical Allele Identifier: CA1772814480

Gene: CHRNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463608T= , CM000670.2:g.27463608T=	GRCh38
NC_000008.10:g.27321125T= , CM000670.1:g.27321125T=	GRCh37
NC_000008.9:g.27377042T=	NCBI36
NG_015827.1:g.20689A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000407991.3:c.835A= MANE Select	ENSP00000385026.1:p.Ile279=
ENST00000637241.1:c.*665A=	ENSP00000490690.1:n.*665A=
ENST00000240132.7:c.790A=	ENSP00000240132.2:p.Ile264=
ENST00000407991.2:c.835A=	ENSP00000385026.1:p.Ile279=
ENST00000520600.1:n.290-1854A=
ENST00000520933.7:c.769A=	ENSP00000429616.2:p.Ile257=
ENST00000523695.5:c.*237A=	ENSP00000430612.1:n.*237A=
NM_000742.3:c.835A=	NP_000733.2:p.Ile279=
NM_001282455.1:c.790A=	NP_001269384.1:p.Ile264=
XM_005273397.1:c.358A=	XP_005273454.1:p.Ile120=
XM_006716282.1:c.835A=	XP_006716345.1:p.Ile279=
XM_011544388.1:c.835A=	XP_011542690.1:p.Ile279=
XM_011544389.1:c.241A=	XP_011542691.1:p.Ile81=
NM_001347705.1:c.358A=	NP_001334634.1:p.Ile120=
NM_001347706.1:c.358A=	NP_001334635.1:p.Ile120=
NM_001347707.1:c.241A=	NP_001334636.1:p.Ile81=
NM_001347708.1:c.241A=	NP_001334637.1:p.Ile81=
XM_011544389.2:c.241A=	XP_011542691.1:p.Ile81=
NM_000742.4:c.835A= MANE Select	NP_000733.2:p.Ile279=
NM_001282455.2:c.790A=	NP_001269384.1:p.Ile264=
NM_001347705.2:c.358A=	NP_001334634.1:p.Ile120=
NM_001347706.2:c.358A=	NP_001334635.1:p.Ile120=
NM_001347707.2:c.241A=	NP_001334636.1:p.Ile81=
NM_001347708.2:c.241A=	NP_001334637.1:p.Ile81=