Canonical Allele Identifier: CA393575627

Gene: CHRNA5

Linked Data

• MyVariant Identifiers: chr15:g.78878989T>A (hg19) ; chr15:g.78586647T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78586647T>A , CM000677.2:g.78586647T>A	GRCh38
NC_000015.9:g.78878989T>A , CM000677.1:g.78878989T>A	GRCh37
NC_000015.8:g.76666044T>A	NCBI36
NG_023328.1:g.26128T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299565.9:c.261T>A MANE Select	ENSP00000299565.5:p.Asp87Glu
ENST00000394802.4:c.76T>A
ENST00000559554.5:c.261T>A	ENSP00000453519.1:p.Asp87Glu
NM_000745.3:c.261T>A	NP_000736.2:p.Asp87Glu
NM_001307945.1:c.261T>A	NP_001294874.1:p.Asp87Glu
XM_005254142.2:c.261T>A	XP_005254199.1:p.Asp87Glu
NM_001307945.2:c.261T>A	NP_001294874.1:p.Asp87Glu
NM_000745.4:c.261T>A MANE Select	NP_000736.2:p.Asp87Glu
NM_001395171.1:c.261T>A	NP_001382100.1:p.Asp87Glu
NM_001395172.1:c.261T>A	NP_001382101.1:p.Asp87Glu
NM_001395173.1:c.261T>A	NP_001382102.1:p.Asp87Glu
NM_001395174.1:c.261T>A	NP_001382103.1:p.Asp87Glu
NM_001395175.1:c.258T>A	NP_001382104.1:p.Asp86Glu