Canonical Allele Identifier: CA393578438
Gene: CHRNA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78590527A>C , CM000677.2:g.78590527A>C GRCh38
NC_000015.9:g.78882869A>C , CM000677.1:g.78882869A>C GRCh37
NC_000015.8:g.76669924A>C NCBI36
NG_023328.1:g.30008A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299565.9:c.1136A>C MANE Select ENSP00000299565.5:p.Glu379Ala
ENST00000394802.4:c.522+429A>C
ENST00000559554.5:c.458+678A>C ENSP00000453519.1:n.458+678A>C
ENST00000559576.1:c.145+21A>C
NM_000745.3:c.1136A>C NP_000736.2:p.Glu379Ala
NM_001307945.1:c.458+678A>C NP_001294874.1:n.458+678A>C
XM_005254142.2:c.707+429A>C XP_005254199.1:n.707+429A>C
NM_001307945.2:c.458+678A>C NP_001294874.1:n.458+678A>C
NM_000745.4:c.1136A>C MANE Select NP_000736.2:p.Glu379Ala
NM_001395171.1:c.1115+21A>C NP_001382100.1:n.1115+21A>C
NM_001395172.1:c.591+545A>C NP_001382101.1:n.591+545A>C
NM_001395173.1:c.713+423A>C NP_001382102.1:n.713+423A>C
NM_001395174.1:c.707+429A>C NP_001382103.1:n.707+429A>C
NM_001395175.1:c.455+678A>C NP_001382104.1:n.455+678A>C