Canonical Allele Identifier: CA349340926

Gene: CHRNA1

Linked Data

• MyVariant Identifiers: chr2:g.175618974G>C (hg19) ; chr2:g.174754246G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174754246G>C , CM000664.2:g.174754246G>C	GRCh38
NC_000002.11:g.175618974G>C , CM000664.1:g.175618974G>C	GRCh37
NC_000002.10:g.175327220G>C	NCBI36
NG_008172.1:g.15227C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636168.2:c.24C>G	ENSP00000490338.2:p.Tyr8Ter
ENST00000672640.1:c.24C>G	ENSP00000500507.1:p.Tyr8Ter
ENST00000261007.9:c.588C>G	ENSP00000261007.5:p.Tyr196Ter
ENST00000348749.9:c.513C>G MANE Select	ENSP00000261008.5:p.Tyr171Ter
ENST00000409219.5:c.513C>G	ENSP00000386611.1:p.Tyr171Ter
ENST00000409323.1:c.513C>G	ENSP00000386684.1:p.Tyr171Ter
ENST00000409542.5:c.267C>G	ENSP00000387026.1:p.Tyr89Ter
ENST00000435083.5:c.*157C>G	ENSP00000395805.1:n.*157C>G
NM_000079.3:c.513C>G	NP_000070.1:p.Tyr171Ter
NM_001039523.2:c.588C>G	NP_001034612.1:p.Tyr196Ter
XM_017003256.1:c.609C>G	XP_016858745.1:p.Tyr203Ter
XM_017003257.1:c.534C>G	XP_016858746.1:p.Tyr178Ter
NM_000079.4:c.513C>G MANE Select	NP_000070.1:p.Tyr171Ter
NM_001039523.3:c.588C>G	NP_001034612.1:p.Tyr196Ter