Canonical Allele Identifier: CA430022327

Gene: CHRNA1

Linked Data

• MyVariant Identifiers: chr2:g.175614767C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174750039C>A , CM000664.2:g.174750039C>A	GRCh38
NC_000002.11:g.175614767C>A , CM000664.1:g.175614767C>A	GRCh37
NC_000002.10:g.175323013C>A	NCBI36
NG_008172.1:g.19434G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000636168.2:c.420G>T	ENSP00000490338.2:p.Val140=
ENST00000672640.1:c.420G>T	ENSP00000500507.1:p.Val140=
ENST00000261007.9:c.984G>T	ENSP00000261007.5:p.Val328=
ENST00000348749.9:c.909G>T MANE Select	ENSP00000261008.5:p.Val303=
ENST00000409219.5:c.909G>T	ENSP00000386611.1:p.Val303=
ENST00000409542.5:c.663G>T	ENSP00000387026.1:p.Val221=
ENST00000435083.5:c.*553G>T	ENSP00000395805.1:n.*553G>T
NM_000079.3:c.909G>T	NP_000070.1:p.Val303=
NM_001039523.2:c.984G>T	NP_001034612.1:p.Val328=
XM_017003256.1:c.1005G>T	XP_016858745.1:p.Val335=
XM_017003257.1:c.930G>T	XP_016858746.1:p.Val310=
NM_000079.4:c.909G>T MANE Select	NP_000070.1:p.Val303=
NM_001039523.3:c.984G>T	NP_001034612.1:p.Val328=