Canonical Allele Identifier: CA1772813565

Gene: CHRNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463183_27463184delinsCT , CM000670.2:g.27463183_27463184delinsCT	GRCh38
NC_000008.10:g.27320700_27320701delinsCT , CM000670.1:g.27320700_27320701delinsCT	GRCh37
NC_000008.9:g.27376617_27376618delinsCT	NCBI36
NG_015827.1:g.21113_21114delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1259_1260delinsAG MANE Select	ENSP00000385026.1:p.Glu420=
ENST00000240132.7:c.1214_1215delinsAG	ENSP00000240132.2:p.Glu405=
ENST00000407991.2:c.1259_1260delinsAG	ENSP00000385026.1:p.Glu420=
ENST00000520600.1:n.290-1430_290-1429delinsAG
ENST00000520933.7:c.1193_1194delinsAG	ENSP00000429616.2:p.Glu398=
ENST00000523695.5:c.*661_*662delinsAG	ENSP00000430612.1:n.*661_*662delinsAG
NM_000742.3:c.1259_1260delinsAG	NP_000733.2:p.Glu420=
NM_001282455.1:c.1214_1215delinsAG	NP_001269384.1:p.Glu405=
XM_005273397.1:c.782_783delinsAG	XP_005273454.1:p.Glu261=
XM_006716282.1:c.1259_1260delinsAG	XP_006716345.1:p.Glu420=
XM_011544388.1:c.1259_1260delinsAG	XP_011542690.1:p.Glu420=
XM_011544389.1:c.665_666delinsAG	XP_011542691.1:p.Glu222=
NM_001347705.1:c.782_783delinsAG	NP_001334634.1:p.Glu261=
NM_001347706.1:c.782_783delinsAG	NP_001334635.1:p.Glu261=
NM_001347707.1:c.665_666delinsAG	NP_001334636.1:p.Glu222=
NM_001347708.1:c.665_666delinsAG	NP_001334637.1:p.Glu222=
XM_011544389.2:c.665_666delinsAG	XP_011542691.1:p.Glu222=
NM_000742.4:c.1259_1260delinsAG MANE Select	NP_000733.2:p.Glu420=
NM_001282455.2:c.1214_1215delinsAG	NP_001269384.1:p.Glu405=
NM_001347705.2:c.782_783delinsAG	NP_001334634.1:p.Glu261=
NM_001347706.2:c.782_783delinsAG	NP_001334635.1:p.Glu261=
NM_001347707.2:c.665_666delinsAG	NP_001334636.1:p.Glu222=
NM_001347708.2:c.665_666delinsAG	NP_001334637.1:p.Glu222=