Canonical Allele Identifier: CA1772814545

Gene: CHRNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463674A= , CM000670.2:g.27463674A=	GRCh38
NC_000008.10:g.27321191A= , CM000670.1:g.27321191A=	GRCh37
NC_000008.9:g.27377108A=	NCBI36
NG_015827.1:g.20623T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000407991.3:c.769T= MANE Select	ENSP00000385026.1:p.Tyr257=
ENST00000637241.1:c.*599T=	ENSP00000490690.1:n.*599T=
ENST00000240132.7:c.724T=	ENSP00000240132.2:p.Tyr242=
ENST00000407991.2:c.769T=	ENSP00000385026.1:p.Tyr257=
ENST00000520600.1:n.290-1920T=
ENST00000520933.7:c.703T=	ENSP00000429616.2:p.Tyr235=
ENST00000522008.1:n.499T=
ENST00000523695.5:c.*171T=	ENSP00000430612.1:n.*171T=
NM_000742.3:c.769T=	NP_000733.2:p.Tyr257=
NM_001282455.1:c.724T=	NP_001269384.1:p.Tyr242=
XM_005273397.1:c.292T=	XP_005273454.1:p.Tyr98=
XM_006716282.1:c.769T=	XP_006716345.1:p.Tyr257=
XM_011544388.1:c.769T=	XP_011542690.1:p.Tyr257=
XM_011544389.1:c.175T=	XP_011542691.1:p.Tyr59=
NM_001347705.1:c.292T=	NP_001334634.1:p.Tyr98=
NM_001347706.1:c.292T=	NP_001334635.1:p.Tyr98=
NM_001347707.1:c.175T=	NP_001334636.1:p.Tyr59=
NM_001347708.1:c.175T=	NP_001334637.1:p.Tyr59=
XM_011544389.2:c.175T=	XP_011542691.1:p.Tyr59=
NM_000742.4:c.769T= MANE Select	NP_000733.2:p.Tyr257=
NM_001282455.2:c.724T=	NP_001269384.1:p.Tyr242=
NM_001347705.2:c.292T=	NP_001334634.1:p.Tyr98=
NM_001347706.2:c.292T=	NP_001334635.1:p.Tyr98=
NM_001347707.2:c.175T=	NP_001334636.1:p.Tyr59=
NM_001347708.2:c.175T=	NP_001334637.1:p.Tyr59=