Canonical Allele Identifier: CA2168283222

Gene: CHRNA7

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32126544C>G , CM000677.2:g.32126544C>G	GRCh38
NC_000015.9:g.32418745C>G , CM000677.1:g.32418745C>G	GRCh37
NC_000015.8:g.30206037C>G	NCBI36
NG_009216.1:g.101020C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306901.9:c.350+14645C>G MANE Select	ENSP00000303727.2:n.350+14645C>G
ENST00000635722.1:c.196-30912C>G	ENSP00000490605.1:n.196-30912C>G
ENST00000635884.1:c.164+14645C>G	ENSP00000489834.1:n.164+14645C>G
ENST00000635978.1:c.113+14645C>G	ENSP00000490778.1:n.113+14645C>G
ENST00000636044.1:c.350+14645C>G	ENSP00000489970.1:n.350+14645C>G
ENST00000636271.1:c.192+14645C>G
ENST00000636292.1:n.720+14645C>G
ENST00000636440.1:c.371+14645C>G	ENSP00000490366.1:n.371+14645C>G
ENST00000636603.1:c.164+14645C>G	ENSP00000490513.1:n.164+14645C>G
ENST00000636647.1:n.339+14645C>G
ENST00000636850.1:c.340+14645C>G	ENSP00000490906.1:n.340+14645C>G
ENST00000637033.1:c.164+14645C>G	ENSP00000490227.1:n.164+14645C>G
ENST00000637183.1:c.113+14645C>G	ENSP00000490365.1:n.113+14645C>G
ENST00000637350.1:c.474+14181C>G	ENSP00000489911.1:n.474+14181C>G
ENST00000637519.1:c.240+25197C>G	ENSP00000490924.1:n.240+25197C>G
ENST00000637552.1:c.350+14645C>G	ENSP00000490773.1:n.350+14645C>G
ENST00000637971.1:c.477+14181C>G	ENSP00000489919.1:n.477+14181C>G
ENST00000638031.1:c.474+14181C>G	ENSP00000490526.1:n.474+14181C>G
ENST00000638106.1:c.-194+25197C>G	ENSP00000490413.1:n.-194+25197C>G
ENST00000675428.1:c.437+14645C>G	ENSP00000502560.1:n.437+14645C>G
ENST00000676380.1:n.425+14645C>G
ENST00000306901.7:c.350+14645C>G	ENSP00000303727.2:n.350+14645C>G
ENST00000437966.3:c.240+25197C>G	ENSP00000399087.3:n.240+25197C>G
ENST00000454250.7:c.437+14645C>G	ENSP00000407546.3:n.437+14645C>G
NM_000746.5:c.350+14645C>G	NP_000737.1:n.350+14645C>G
NM_001190455.2:c.437+14645C>G	NP_001177384.1:n.437+14645C>G
NR_046324.1:n.352+25197C>G
XM_011521175.1:c.122+14181C>G	XP_011519477.1:n.122+14181C>G
XM_011521176.1:c.113+14645C>G	XP_011519478.1:n.113+14645C>G
XM_011521178.1:c.350+14645C>G	XP_011519480.1:n.350+14645C>G
XM_011521179.1:c.-194+25197C>G	XP_011519481.1:n.-194+25197C>G
XM_011521176.3:c.302+14645C>G	XP_011519478.2:n.302+14645C>G
XM_011521178.3:c.350+14645C>G	XP_011519480.1:n.350+14645C>G
XM_017021882.1:c.167+14181C>G	XP_016877371.1:n.167+14181C>G
XM_017021883.2:c.164+14181C>G	XP_016877372.1:n.164+14181C>G
XM_017021884.1:c.-194+25197C>G	XP_016877373.1:n.-194+25197C>G
NM_000746.6:c.350+14645C>G MANE Select	NP_000737.1:n.350+14645C>G
NM_001190455.3:c.437+14645C>G	NP_001177384.1:n.437+14645C>G