Canonical Allele Identifier: CA491972101

Gene: CHRNA5

Linked Data

• dbSNP Id: rs1287827346
• gnomAD v2: 15-78882846-C-T
• gnomAD v3: 15-78590504-C-T
• gnomAD v4: 15-78590504-C-T
• MyVariant Identifiers: chr15:g.78882846C>T (hg19) ; chr15:g.78590504C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78590504C>T , CM000677.2:g.78590504C>T	GRCh38
NC_000015.9:g.78882846C>T , CM000677.1:g.78882846C>T	GRCh37
NC_000015.8:g.76669901C>T	NCBI36
NG_023328.1:g.29985C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299565.9:c.1113C>T MANE Select	ENSP00000299565.5:p.Asp371=
ENST00000394802.4:c.522+406C>T
ENST00000559554.5:c.458+655C>T	ENSP00000453519.1:n.458+655C>T
ENST00000559576.1:c.143C>T
NM_000745.3:c.1113C>T	NP_000736.2:p.Asp371=
NM_001307945.1:c.458+655C>T	NP_001294874.1:n.458+655C>T
XM_005254142.2:c.707+406C>T	XP_005254199.1:n.707+406C>T
NM_001307945.2:c.458+655C>T	NP_001294874.1:n.458+655C>T
NM_000745.4:c.1113C>T MANE Select	NP_000736.2:p.Asp371=
NM_001395171.1:c.1113C>T	NP_001382100.1:p.Asp371=
NM_001395172.1:c.591+522C>T	NP_001382101.1:n.591+522C>T
NM_001395173.1:c.713+400C>T	NP_001382102.1:n.713+400C>T
NM_001395174.1:c.707+406C>T	NP_001382103.1:n.707+406C>T
NM_001395175.1:c.455+655C>T	NP_001382104.1:n.455+655C>T