Canonical Allele Identifier: CA393577875

Gene: CHRNA5

Linked Data

• dbSNP Id: rs146801604
• MyVariant Identifiers: chr15:g.78882732C>A (hg19) ; chr15:g.78590390C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78590390C>A , CM000677.2:g.78590390C>A	GRCh38
NC_000015.9:g.78882732C>A , CM000677.1:g.78882732C>A	GRCh37
NC_000015.8:g.76669787C>A	NCBI36
NG_023328.1:g.29871C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.999C>A MANE Select	ENSP00000299565.5:p.Phe333Leu
ENST00000394802.4:c.522+292C>A
ENST00000559554.5:c.458+541C>A	ENSP00000453519.1:n.458+541C>A
ENST00000559576.1:c.29C>A
NM_000745.3:c.999C>A	NP_000736.2:p.Phe333Leu
NM_001307945.1:c.458+541C>A	NP_001294874.1:n.458+541C>A
XM_005254142.2:c.707+292C>A	XP_005254199.1:n.707+292C>A
NM_001307945.2:c.458+541C>A	NP_001294874.1:n.458+541C>A
NM_000745.4:c.999C>A MANE Select	NP_000736.2:p.Phe333Leu
NM_001395171.1:c.999C>A	NP_001382100.1:p.Phe333Leu
NM_001395172.1:c.591+408C>A	NP_001382101.1:n.591+408C>A
NM_001395173.1:c.713+286C>A	NP_001382102.1:n.713+286C>A
NM_001395174.1:c.707+292C>A	NP_001382103.1:n.707+292C>A
NM_001395175.1:c.455+541C>A	NP_001382104.1:n.455+541C>A