Canonical Allele Identifier: CA393577904

Gene: CHRNA5

Linked Data

• MyVariant Identifiers: chr15:g.78882739A>C (hg19) ; chr15:g.78590397A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78590397A>C , CM000677.2:g.78590397A>C	GRCh38
NC_000015.9:g.78882739A>C , CM000677.1:g.78882739A>C	GRCh37
NC_000015.8:g.76669794A>C	NCBI36
NG_023328.1:g.29878A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.1006A>C MANE Select	ENSP00000299565.5:p.Asn336His
ENST00000394802.4:c.522+299A>C
ENST00000559554.5:c.458+548A>C	ENSP00000453519.1:n.458+548A>C
ENST00000559576.1:c.36A>C
NM_000745.3:c.1006A>C	NP_000736.2:p.Asn336His
NM_001307945.1:c.458+548A>C	NP_001294874.1:n.458+548A>C
XM_005254142.2:c.707+299A>C	XP_005254199.1:n.707+299A>C
NM_001307945.2:c.458+548A>C	NP_001294874.1:n.458+548A>C
NM_000745.4:c.1006A>C MANE Select	NP_000736.2:p.Asn336His
NM_001395171.1:c.1006A>C	NP_001382100.1:p.Asn336His
NM_001395172.1:c.591+415A>C	NP_001382101.1:n.591+415A>C
NM_001395173.1:c.713+293A>C	NP_001382102.1:n.713+293A>C
NM_001395174.1:c.707+299A>C	NP_001382103.1:n.707+299A>C
NM_001395175.1:c.455+548A>C	NP_001382104.1:n.455+548A>C