Canonical Allele Identifier: CA1772813929

Gene: CHRNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463340C= , CM000670.2:g.27463340C=	GRCh38
NC_000008.10:g.27320857C= , CM000670.1:g.27320857C=	GRCh37
NC_000008.9:g.27376774C=	NCBI36
NG_015827.1:g.20957G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1103G= MANE Select	ENSP00000385026.1:p.Gly368=
ENST00000240132.7:c.1058G=	ENSP00000240132.2:p.Gly353=
ENST00000407991.2:c.1103G=	ENSP00000385026.1:p.Gly368=
ENST00000520600.1:n.290-1586G=
ENST00000520933.7:c.1037G=	ENSP00000429616.2:p.Gly346=
ENST00000523695.5:c.*505G=	ENSP00000430612.1:n.*505G=
NM_000742.3:c.1103G=	NP_000733.2:p.Gly368=
NM_001282455.1:c.1058G=	NP_001269384.1:p.Gly353=
XM_005273397.1:c.626G=	XP_005273454.1:p.Gly209=
XM_006716282.1:c.1103G=	XP_006716345.1:p.Gly368=
XM_011544388.1:c.1103G=	XP_011542690.1:p.Gly368=
XM_011544389.1:c.509G=	XP_011542691.1:p.Gly170=
NM_001347705.1:c.626G=	NP_001334634.1:p.Gly209=
NM_001347706.1:c.626G=	NP_001334635.1:p.Gly209=
NM_001347707.1:c.509G=	NP_001334636.1:p.Gly170=
NM_001347708.1:c.509G=	NP_001334637.1:p.Gly170=
XM_011544389.2:c.509G=	XP_011542691.1:p.Gly170=
NM_000742.4:c.1103G= MANE Select	NP_000733.2:p.Gly368=
NM_001282455.2:c.1058G=	NP_001269384.1:p.Gly353=
NM_001347705.2:c.626G=	NP_001334634.1:p.Gly209=
NM_001347706.2:c.626G=	NP_001334635.1:p.Gly209=
NM_001347707.2:c.509G=	NP_001334636.1:p.Gly170=
NM_001347708.2:c.509G=	NP_001334637.1:p.Gly170=