Canonical Allele Identifier: CA393575672

Gene: CHRNA5

Linked Data

• gnomAD v4: 15-78586664-T-G
• MyVariant Identifiers: chr15:g.78879006T>G (hg19) ; chr15:g.78586664T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78586664T>G , CM000677.2:g.78586664T>G	GRCh38
NC_000015.9:g.78879006T>G , CM000677.1:g.78879006T>G	GRCh37
NC_000015.8:g.76666061T>G	NCBI36
NG_023328.1:g.26145T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.278T>G MANE Select	ENSP00000299565.5:p.Met93Arg
ENST00000394802.4:c.93T>G
ENST00000559554.5:c.278T>G	ENSP00000453519.1:p.Met93Arg
NM_000745.3:c.278T>G	NP_000736.2:p.Met93Arg
NM_001307945.1:c.278T>G	NP_001294874.1:p.Met93Arg
XM_005254142.2:c.278T>G	XP_005254199.1:p.Met93Arg
NM_001307945.2:c.278T>G	NP_001294874.1:p.Met93Arg
NM_000745.4:c.278T>G MANE Select	NP_000736.2:p.Met93Arg
NM_001395171.1:c.278T>G	NP_001382100.1:p.Met93Arg
NM_001395172.1:c.278T>G	NP_001382101.1:p.Met93Arg
NM_001395173.1:c.278T>G	NP_001382102.1:p.Met93Arg
NM_001395174.1:c.278T>G	NP_001382103.1:p.Met93Arg
NM_001395175.1:c.275T>G	NP_001382104.1:p.Met92Arg