Canonical Allele Identifier: CA460186506

Gene: CHRNA2

Linked Data

• MyVariant Identifiers: chr8:g.27320855_27320856insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463338_27463339insG , CM000670.2:g.27463338_27463339insG	GRCh38
NC_000008.10:g.27320855_27320856insG , CM000670.1:g.27320855_27320856insG	GRCh37
NC_000008.9:g.27376772_27376773insG	NCBI36
NG_015827.1:g.20958_20959insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1104_1105insC MANE Select	ENSP00000385026.1:p.Ala369ArgfsTer?
ENST00000240132.7:c.1059_1060insC	ENSP00000240132.2:p.Ala354ArgfsTer?
ENST00000407991.2:c.1104_1105insC	ENSP00000385026.1:p.Ala369ArgfsTer?
ENST00000520600.1:n.290-1585_290-1584insC
ENST00000520933.7:c.1038_1039insC	ENSP00000429616.2:p.Ala347ArgfsTer?
ENST00000523695.5:c.*506_*507insC	ENSP00000430612.1:n.*506_*507insC
NM_000742.3:c.1104_1105insC	NP_000733.2:p.Ala369ArgfsTer?
NM_001282455.1:c.1059_1060insC	NP_001269384.1:p.Ala354ArgfsTer?
XM_005273397.1:c.627_628insC	XP_005273454.1:p.Ala210ArgfsTer?
XM_006716282.1:c.1104_1105insC	XP_006716345.1:p.Ala369ArgfsTer?
XM_011544388.1:c.1104_1105insC	XP_011542690.1:p.Ala369ArgfsTer?
XM_011544389.1:c.510_511insC	XP_011542691.1:p.Ala171ArgfsTer?
NM_001347705.1:c.627_628insC	NP_001334634.1:p.Ala210ArgfsTer?
NM_001347706.1:c.627_628insC	NP_001334635.1:p.Ala210ArgfsTer?
NM_001347707.1:c.510_511insC	NP_001334636.1:p.Ala171ArgfsTer?
NM_001347708.1:c.510_511insC	NP_001334637.1:p.Ala171ArgfsTer?
XM_011544389.2:c.510_511insC	XP_011542691.1:p.Ala171ArgfsTer?
NM_000742.4:c.1104_1105insC MANE Select	NP_000733.2:p.Ala369ArgfsTer?
NM_001282455.2:c.1059_1060insC	NP_001269384.1:p.Ala354ArgfsTer?
NM_001347705.2:c.627_628insC	NP_001334634.1:p.Ala210ArgfsTer?
NM_001347706.2:c.627_628insC	NP_001334635.1:p.Ala210ArgfsTer?
NM_001347707.2:c.510_511insC	NP_001334636.1:p.Ala171ArgfsTer?
NM_001347708.2:c.510_511insC	NP_001334637.1:p.Ala171ArgfsTer?