Canonical Allele Identifier: CA268576686

Gene: CHRNA7

Linked Data

• dbSNP Id: rs989710517
• gnomAD v3: 15-32065526-C-T
• gnomAD v4: 15-32065526-C-T
• MyVariant Identifiers: chr15:g.32357729C>T (hg19) ; chr15:g.32065526C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32065526C>T , CM000677.2:g.32065526C>T	GRCh38
NC_000015.9:g.32357729C>T , CM000677.1:g.32357729C>T	GRCh37
NC_000015.8:g.30145021C>T	NCBI36
NG_009216.1:g.40004C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306901.9:c.195+34489C>T MANE Select	ENSP00000303727.2:n.195+34489C>T
ENST00000635722.1:c.195+34489C>T	ENSP00000490605.1:n.195+34489C>T
ENST00000635759.1:c.61+34489C>T
ENST00000635884.1:c.9+34489C>T	ENSP00000489834.1:n.9+34489C>T
ENST00000635978.1:c.-42-35777C>T	ENSP00000490778.1:n.-42-35777C>T
ENST00000636044.1:c.195+34489C>T	ENSP00000489970.1:n.195+34489C>T
ENST00000636271.1:c.37+34489C>T
ENST00000636295.1:n.195+34489C>T
ENST00000636440.1:c.216+34489C>T	ENSP00000490366.1:n.216+34489C>T
ENST00000636603.1:c.9+34489C>T	ENSP00000490513.1:n.9+34489C>T
ENST00000636647.1:n.184+34489C>T
ENST00000636850.1:c.195+34489C>T	ENSP00000490906.1:n.195+34489C>T
ENST00000637033.1:c.9+34489C>T	ENSP00000490227.1:n.9+34489C>T
ENST00000637183.1:c.-42-35777C>T	ENSP00000490365.1:n.-42-35777C>T
ENST00000637350.1:c.195+34489C>T	ENSP00000489911.1:n.195+34489C>T
ENST00000637519.1:c.195+34489C>T	ENSP00000490924.1:n.195+34489C>T
ENST00000637552.1:c.195+34489C>T	ENSP00000490773.1:n.195+34489C>T
ENST00000637786.2:c.195+34489C>T	ENSP00000490015.1:n.195+34489C>T
ENST00000637971.1:c.195+34489C>T	ENSP00000489919.1:n.195+34489C>T
ENST00000638031.1:c.195+34489C>T	ENSP00000490526.1:n.195+34489C>T
ENST00000638106.1:c.-239+34489C>T	ENSP00000490413.1:n.-239+34489C>T
ENST00000675428.1:c.282+34489C>T	ENSP00000502560.1:n.282+34489C>T
ENST00000306901.7:c.195+34489C>T	ENSP00000303727.2:n.195+34489C>T
ENST00000437966.3:c.195+34489C>T	ENSP00000399087.3:n.195+34489C>T
ENST00000454250.7:c.282+34489C>T	ENSP00000407546.3:n.282+34489C>T
NM_000746.5:c.195+34489C>T	NP_000737.1:n.195+34489C>T
NM_001190455.2:c.282+34489C>T	NP_001177384.1:n.282+34489C>T
NR_046324.1:n.307+34489C>T
XM_011521178.1:c.195+34489C>T	XP_011519480.1:n.195+34489C>T
XM_011521179.1:c.-239+34489C>T	XP_011519481.1:n.-239+34489C>T
XM_011521178.3:c.195+34489C>T	XP_011519480.1:n.195+34489C>T
XM_017021882.1:c.-116+34489C>T	XP_016877371.1:n.-116+34489C>T
XM_017021883.2:c.-116+34489C>T	XP_016877372.1:n.-116+34489C>T
XM_017021884.1:c.-239+34489C>T	XP_016877373.1:n.-239+34489C>T
NM_000746.6:c.195+34489C>T MANE Select	NP_000737.1:n.195+34489C>T
NM_001190455.3:c.282+34489C>T	NP_001177384.1:n.282+34489C>T