Canonical Allele Identifier: CA2730841657

Gene: CHRNA7

Linked Data

• dbSNP Id: rs2141361923

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32152251T>C , CM000677.2:g.32152251T>C	GRCh38
NC_000015.9:g.32444452T>C , CM000677.1:g.32444452T>C	GRCh37
NC_000015.8:g.30231744T>C	NCBI36
NG_009216.1:g.126727T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306901.9:c.351-1656T>C MANE Select	ENSP00000303727.2:n.351-1656T>C
ENST00000635722.1:c.196-5205T>C	ENSP00000490605.1:n.196-5205T>C
ENST00000635884.1:c.165-1656T>C	ENSP00000489834.1:n.165-1656T>C
ENST00000635978.1:c.114-1656T>C	ENSP00000490778.1:n.114-1656T>C
ENST00000636044.1:c.351-5357T>C	ENSP00000489970.1:n.351-5357T>C
ENST00000636271.1:c.193-1656T>C
ENST00000636292.1:n.721-1656T>C
ENST00000636440.1:c.372-1656T>C	ENSP00000490366.1:n.372-1656T>C
ENST00000636603.1:c.165-1656T>C	ENSP00000490513.1:n.165-1656T>C
ENST00000636647.1:n.340-1656T>C
ENST00000636850.1:c.341-1656T>C	ENSP00000490906.1:n.341-1656T>C
ENST00000637033.1:c.165-1656T>C	ENSP00000490227.1:n.165-1656T>C
ENST00000637183.1:c.114-1656T>C	ENSP00000490365.1:n.114-1656T>C
ENST00000637350.1:c.475-5357T>C	ENSP00000489911.1:n.475-5357T>C
ENST00000637519.1:c.241-1656T>C	ENSP00000490924.1:n.241-1656T>C
ENST00000637552.1:c.351-1656T>C	ENSP00000490773.1:n.351-1656T>C
ENST00000637971.1:c.478-1656T>C	ENSP00000489919.1:n.478-1656T>C
ENST00000638031.1:c.475-1656T>C	ENSP00000490526.1:n.475-1656T>C
ENST00000638106.1:c.-193-1656T>C	ENSP00000490413.1:n.-193-1656T>C
ENST00000675428.1:c.438-1656T>C	ENSP00000502560.1:n.438-1656T>C
ENST00000676380.1:n.426-1656T>C
ENST00000306901.7:c.351-1656T>C	ENSP00000303727.2:n.351-1656T>C
ENST00000437966.3:c.241-5357T>C	ENSP00000399087.3:n.241-5357T>C
ENST00000454250.7:c.438-1656T>C	ENSP00000407546.3:n.438-1656T>C
NM_000746.5:c.351-1656T>C	NP_000737.1:n.351-1656T>C
NM_001190455.2:c.438-1656T>C	NP_001177384.1:n.438-1656T>C
NR_046324.1:n.353-5357T>C
XM_011521175.1:c.123-1656T>C	XP_011519477.1:n.123-1656T>C
XM_011521176.1:c.114-1656T>C	XP_011519478.1:n.114-1656T>C
XM_011521177.1:c.48-1656T>C	XP_011519479.1:n.48-1656T>C
XM_011521178.1:c.351-1656T>C	XP_011519480.1:n.351-1656T>C
XM_011521179.1:c.-193-1656T>C	XP_011519481.1:n.-193-1656T>C
XM_011521176.3:c.303-1656T>C	XP_011519478.2:n.303-1656T>C
XM_011521177.2:c.48-1656T>C	XP_011519479.1:n.48-1656T>C
XM_011521178.3:c.351-1656T>C	XP_011519480.1:n.351-1656T>C
XM_017021882.1:c.168-1656T>C	XP_016877371.1:n.168-1656T>C
XM_017021883.2:c.165-1656T>C	XP_016877372.1:n.165-1656T>C
XM_017021884.1:c.-193-1656T>C	XP_016877373.1:n.-193-1656T>C
NM_000746.6:c.351-1656T>C MANE Select	NP_000737.1:n.351-1656T>C
NM_001190455.3:c.438-1656T>C	NP_001177384.1:n.438-1656T>C