Canonical Allele Identifier: CA2563922189

Gene: CHRNA7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32152011_32152012insGG , CM000677.2:g.32152011_32152012insGG	GRCh38
NC_000015.9:g.32444212_32444213insGG , CM000677.1:g.32444212_32444213insGG	GRCh37
NC_000015.8:g.30231504_30231505insGG	NCBI36
NG_009216.1:g.126487_126488insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000306901.9:c.351-1896_351-1895insGG MANE Select	ENSP00000303727.2:n.351-1896_351-1895insGG
ENST00000635722.1:c.196-5445_196-5444insGG	ENSP00000490605.1:n.196-5445_196-5444insGG
ENST00000635884.1:c.165-1896_165-1895insGG	ENSP00000489834.1:n.165-1896_165-1895insGG
ENST00000635978.1:c.114-1896_114-1895insGG	ENSP00000490778.1:n.114-1896_114-1895insGG
ENST00000636044.1:c.351-5597_351-5596insGG	ENSP00000489970.1:n.351-5597_351-5596insGG
ENST00000636271.1:c.193-1896_193-1895insGG
ENST00000636292.1:n.721-1896_721-1895insGG
ENST00000636440.1:c.372-1896_372-1895insGG	ENSP00000490366.1:n.372-1896_372-1895insGG
ENST00000636603.1:c.165-1896_165-1895insGG	ENSP00000490513.1:n.165-1896_165-1895insGG
ENST00000636647.1:n.340-1896_340-1895insGG
ENST00000636850.1:c.341-1896_341-1895insGG	ENSP00000490906.1:n.341-1896_341-1895insGG
ENST00000637033.1:c.165-1896_165-1895insGG	ENSP00000490227.1:n.165-1896_165-1895insGG
ENST00000637183.1:c.114-1896_114-1895insGG	ENSP00000490365.1:n.114-1896_114-1895insGG
ENST00000637350.1:c.475-5597_475-5596insGG	ENSP00000489911.1:n.475-5597_475-5596insGG
ENST00000637519.1:c.241-1896_241-1895insGG	ENSP00000490924.1:n.241-1896_241-1895insGG
ENST00000637552.1:c.351-1896_351-1895insGG	ENSP00000490773.1:n.351-1896_351-1895insGG
ENST00000637971.1:c.478-1896_478-1895insGG	ENSP00000489919.1:n.478-1896_478-1895insGG
ENST00000638031.1:c.475-1896_475-1895insGG	ENSP00000490526.1:n.475-1896_475-1895insGG
ENST00000638106.1:c.-193-1896_-193-1895insGG	ENSP00000490413.1:n.-193-1896_-193-1895insGG
ENST00000675428.1:c.438-1896_438-1895insGG	ENSP00000502560.1:n.438-1896_438-1895insGG
ENST00000676380.1:n.426-1896_426-1895insGG
ENST00000306901.7:c.351-1896_351-1895insGG	ENSP00000303727.2:n.351-1896_351-1895insGG
ENST00000437966.3:c.241-5597_241-5596insGG	ENSP00000399087.3:n.241-5597_241-5596insGG
ENST00000454250.7:c.438-1896_438-1895insGG	ENSP00000407546.3:n.438-1896_438-1895insGG
NM_000746.5:c.351-1896_351-1895insGG	NP_000737.1:n.351-1896_351-1895insGG
NM_001190455.2:c.438-1896_438-1895insGG	NP_001177384.1:n.438-1896_438-1895insGG
NR_046324.1:n.353-5597_353-5596insGG
XM_011521175.1:c.123-1896_123-1895insGG	XP_011519477.1:n.123-1896_123-1895insGG
XM_011521176.1:c.114-1896_114-1895insGG	XP_011519478.1:n.114-1896_114-1895insGG
XM_011521177.1:c.48-1896_48-1895insGG	XP_011519479.1:n.48-1896_48-1895insGG
XM_011521178.1:c.351-1896_351-1895insGG	XP_011519480.1:n.351-1896_351-1895insGG
XM_011521179.1:c.-193-1896_-193-1895insGG	XP_011519481.1:n.-193-1896_-193-1895insGG
XM_011521176.3:c.303-1896_303-1895insGG	XP_011519478.2:n.303-1896_303-1895insGG
XM_011521177.2:c.48-1896_48-1895insGG	XP_011519479.1:n.48-1896_48-1895insGG
XM_011521178.3:c.351-1896_351-1895insGG	XP_011519480.1:n.351-1896_351-1895insGG
XM_017021882.1:c.168-1896_168-1895insGG	XP_016877371.1:n.168-1896_168-1895insGG
XM_017021883.2:c.165-1896_165-1895insGG	XP_016877372.1:n.165-1896_165-1895insGG
XM_017021884.1:c.-193-1896_-193-1895insGG	XP_016877373.1:n.-193-1896_-193-1895insGG
NM_000746.6:c.351-1896_351-1895insGG MANE Select	NP_000737.1:n.351-1896_351-1895insGG
NM_001190455.3:c.438-1896_438-1895insGG	NP_001177384.1:n.438-1896_438-1895insGG