Canonical Allele Identifier: CA971788091

Gene: CHRNA5

Linked Data

• dbSNP Id: rs2052957990
• gnomAD v3: 15-78585993-T-A
• gnomAD v4: 15-78585993-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78585993T>A , CM000677.2:g.78585993T>A	GRCh38
NC_000015.9:g.78878335T>A , CM000677.1:g.78878335T>A	GRCh37
NC_000015.8:g.76665390T>A	NCBI36
NG_023328.1:g.25474T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.259-652T>A MANE Select	ENSP00000299565.5:n.259-652T>A
ENST00000394802.4:c.74-652T>A
ENST00000559554.5:c.259-652T>A	ENSP00000453519.1:n.259-652T>A
NM_000745.3:c.259-652T>A	NP_000736.2:n.259-652T>A
NM_001307945.1:c.259-652T>A	NP_001294874.1:n.259-652T>A
XM_005254142.2:c.259-652T>A	XP_005254199.1:n.259-652T>A
NM_001307945.2:c.259-652T>A	NP_001294874.1:n.259-652T>A
NM_000745.4:c.259-652T>A MANE Select	NP_000736.2:n.259-652T>A
NM_001395171.1:c.259-652T>A	NP_001382100.1:n.259-652T>A
NM_001395172.1:c.259-652T>A	NP_001382101.1:n.259-652T>A
NM_001395173.1:c.259-652T>A	NP_001382102.1:n.259-652T>A
NM_001395174.1:c.259-652T>A	NP_001382103.1:n.259-652T>A
NM_001395175.1:c.256-652T>A	NP_001382104.1:n.256-652T>A