Canonical Allele Identifier: CA349340893

Gene: CHRNA1

Linked Data

• MyVariant Identifiers: chr2:g.175618969C>T (hg19) ; chr2:g.174754241C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174754241C>T , CM000664.2:g.174754241C>T	GRCh38
NC_000002.11:g.175618969C>T , CM000664.1:g.175618969C>T	GRCh37
NC_000002.10:g.175327215C>T	NCBI36
NG_008172.1:g.15232G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.29G>A	ENSP00000490338.2:p.Gly10Asp
ENST00000672640.1:c.29G>A	ENSP00000500507.1:p.Gly10Asp
ENST00000261007.9:c.593G>A	ENSP00000261007.5:p.Gly198Asp
ENST00000348749.9:c.518G>A MANE Select	ENSP00000261008.5:p.Gly173Asp
ENST00000409219.5:c.518G>A	ENSP00000386611.1:p.Gly173Asp
ENST00000409323.1:c.518G>A	ENSP00000386684.1:p.Gly173Asp
ENST00000409542.5:c.272G>A	ENSP00000387026.1:p.Gly91Asp
ENST00000435083.5:c.*162G>A	ENSP00000395805.1:n.*162G>A
NM_000079.3:c.518G>A	NP_000070.1:p.Gly173Asp
NM_001039523.2:c.593G>A	NP_001034612.1:p.Gly198Asp
XM_017003256.1:c.614G>A	XP_016858745.1:p.Gly205Asp
XM_017003257.1:c.539G>A	XP_016858746.1:p.Gly180Asp
NM_000079.4:c.518G>A MANE Select	NP_000070.1:p.Gly173Asp
NM_001039523.3:c.593G>A	NP_001034612.1:p.Gly198Asp