Canonical Allele Identifier: CA370811068

Gene: CHRNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463767A>T , CM000670.2:g.27463767A>T	GRCh38
NC_000008.10:g.27321284A>T , CM000670.1:g.27321284A>T	GRCh37
NC_000008.9:g.27377201A>T	NCBI36
NG_015827.1:g.20530T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.676T>A MANE Select	ENSP00000385026.1:p.Trp226Arg
ENST00000637241.1:c.*506T>A	ENSP00000490690.1:n.*506T>A
ENST00000240132.7:c.631T>A	ENSP00000240132.2:p.Trp211Arg
ENST00000407991.2:c.676T>A	ENSP00000385026.1:p.Trp226Arg
ENST00000520600.1:n.290-2013T>A
ENST00000520933.7:c.610T>A	ENSP00000429616.2:p.Trp204Arg
ENST00000522008.1:n.406T>A
ENST00000523695.5:c.*78T>A	ENSP00000430612.1:n.*78T>A
NM_000742.3:c.676T>A	NP_000733.2:p.Trp226Arg
NM_001282455.1:c.631T>A	NP_001269384.1:p.Trp211Arg
XM_005273397.1:c.199T>A	XP_005273454.1:p.Trp67Arg
XM_006716282.1:c.676T>A	XP_006716345.1:p.Trp226Arg
XM_011544388.1:c.676T>A	XP_011542690.1:p.Trp226Arg
XM_011544389.1:c.82T>A	XP_011542691.1:p.Trp28Arg
NM_001347705.1:c.199T>A	NP_001334634.1:p.Trp67Arg
NM_001347706.1:c.199T>A	NP_001334635.1:p.Trp67Arg
NM_001347707.1:c.82T>A	NP_001334636.1:p.Trp28Arg
NM_001347708.1:c.82T>A	NP_001334637.1:p.Trp28Arg
XM_011544389.2:c.82T>A	XP_011542691.1:p.Trp28Arg
NM_000742.4:c.676T>A MANE Select	NP_000733.2:p.Trp226Arg
NM_001282455.2:c.631T>A	NP_001269384.1:p.Trp211Arg
NM_001347705.2:c.199T>A	NP_001334634.1:p.Trp67Arg
NM_001347706.2:c.199T>A	NP_001334635.1:p.Trp67Arg
NM_001347707.2:c.82T>A	NP_001334636.1:p.Trp28Arg
NM_001347708.2:c.82T>A	NP_001334637.1:p.Trp28Arg