Canonical Allele Identifier: CA491971924

Gene: CHRNA5

Linked Data

• MyVariant Identifiers: chr15:g.78882825T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78590483T>G , CM000677.2:g.78590483T>G	GRCh38
NC_000015.9:g.78882825T>G , CM000677.1:g.78882825T>G	GRCh37
NC_000015.8:g.76669880T>G	NCBI36
NG_023328.1:g.29964T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299565.9:c.1092T>G MANE Select	ENSP00000299565.5:p.Leu364=
ENST00000394802.4:c.522+385T>G
ENST00000559554.5:c.458+634T>G	ENSP00000453519.1:n.458+634T>G
ENST00000559576.1:c.122T>G
NM_000745.3:c.1092T>G	NP_000736.2:p.Leu364=
NM_001307945.1:c.458+634T>G	NP_001294874.1:n.458+634T>G
XM_005254142.2:c.707+385T>G	XP_005254199.1:n.707+385T>G
NM_001307945.2:c.458+634T>G	NP_001294874.1:n.458+634T>G
NM_000745.4:c.1092T>G MANE Select	NP_000736.2:p.Leu364=
NM_001395171.1:c.1092T>G	NP_001382100.1:p.Leu364=
NM_001395172.1:c.591+501T>G	NP_001382101.1:n.591+501T>G
NM_001395173.1:c.713+379T>G	NP_001382102.1:n.713+379T>G
NM_001395174.1:c.707+385T>G	NP_001382103.1:n.707+385T>G
NM_001395175.1:c.455+634T>G	NP_001382104.1:n.455+634T>G