Canonical Allele Identifier: CA430023028

Gene: CHRNA1

Linked Data

• MyVariant Identifiers: chr2:g.175618965A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174754237A>C , CM000664.2:g.174754237A>C	GRCh38
NC_000002.11:g.175618965A>C , CM000664.1:g.175618965A>C	GRCh37
NC_000002.10:g.175327211A>C	NCBI36
NG_008172.1:g.15236T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.33T>G	ENSP00000490338.2:p.Ser11=
ENST00000672640.1:c.33T>G	ENSP00000500507.1:p.Ser11=
ENST00000261007.9:c.597T>G	ENSP00000261007.5:p.Ser199=
ENST00000348749.9:c.522T>G MANE Select	ENSP00000261008.5:p.Ser174=
ENST00000409219.5:c.522T>G	ENSP00000386611.1:p.Ser174=
ENST00000409323.1:c.522T>G	ENSP00000386684.1:p.Ser174=
ENST00000409542.5:c.276T>G	ENSP00000387026.1:p.Ser92=
ENST00000435083.5:c.*166T>G	ENSP00000395805.1:n.*166T>G
NM_000079.3:c.522T>G	NP_000070.1:p.Ser174=
NM_001039523.2:c.597T>G	NP_001034612.1:p.Ser199=
XM_017003256.1:c.618T>G	XP_016858745.1:p.Ser206=
XM_017003257.1:c.543T>G	XP_016858746.1:p.Ser181=
NM_000079.4:c.522T>G MANE Select	NP_000070.1:p.Ser174=
NM_001039523.3:c.597T>G	NP_001034612.1:p.Ser199=